Year |
Citation |
Score |
2023 |
Lu MZ, Loh TP. Development and Applications of Water-Compatible Reactions: A Journey to Be Continued. Accounts of Chemical Research. 57: 70-92. PMID 38112292 DOI: 10.1021/acs.accounts.3c00555 |
0.308 |
|
2023 |
Wang Y, Wu G, Yan K, Qin J, Liu R, Rong N, Tang Y, Loh TP, Xie P. Sulfination of Unactivated Allylic Alcohols via Sulfinate-Sulfone Rearrangement. Organic Letters. PMID 38059565 DOI: 10.1021/acs.orglett.3c03709 |
0.357 |
|
2023 |
Tian JS, Xu SW, Bi YH, Cao ZZ, Loh TP. Oxidative Amination of Aldehydes with Amines into α-Amino Ketones. Organic Letters. 25: 8922-8926. PMID 38057263 DOI: 10.1021/acs.orglett.3c03771 |
0.313 |
|
2023 |
Wang Y, Feng J, Li EQ, Jia Z, Loh TP. Recent advances in ligand-enabled palladium-catalyzed divergent synthesis. Organic & Biomolecular Chemistry. PMID 38050418 DOI: 10.1039/d3ob01679j |
0.368 |
|
2023 |
Zeng W, Zhang X, Zhang Y, Xiao S, Tang Y, Xie P, Loh TP. Organophotoredox-Catalyzed Intermolecular Formal Grob Fragmentation of Cyclic Alcohols with Activated Allylic Acetates. Organic Letters. PMID 37515785 DOI: 10.1021/acs.orglett.3c02129 |
0.344 |
|
2023 |
Zhao Y, Wang S, Shao H, Tan X, Chen R, Loh TP, Zhou JS, Wu X. Regioselective and Geometrically Controlled Heck 1,1-Diarylation of Unactivated Aliphatic Alkenes. Organic Letters. PMID 37272667 DOI: 10.1021/acs.orglett.3c01214 |
0.333 |
|
2023 |
Teng S, Ng EWH, Zhang Z, Soon CN, Xu H, Li R, Hirao H, Loh TP. Alkynone β-trifluoroborates: A new class of amine-specific biocompatible click reagents. Science Advances. 9: eadg4924. PMID 37126553 DOI: 10.1126/sciadv.adg4924 |
0.357 |
|
2022 |
Zong X, Liu S, Zhang Z, Ji L, Zhang T, Jia Z, Loh TP. Fluoride Anion Catalyzed Mukaiyama-Aldol Reaction: Rapid Access to α-Fluoro-β-hydroxy Esters. The Journal of Organic Chemistry. PMID 35443775 DOI: 10.1021/acs.joc.2c00240 |
0.346 |
|
2021 |
Hu J, Yang X, Shi S, Cheng B, Luo X, Lan Y, Loh TP. Metal-free C(sp)-H functionalization of sulfonamides strain-release rearrangement. Chemical Science. 12: 4034-4040. PMID 34163674 DOI: 10.1039/d0sc06603f |
0.315 |
|
2021 |
Li B, Zeng W, Wang L, Geng Z, Loh TP, Xie P. Visible-Light-Induced Trifluoromethylation of Allylic Alcohols. Organic Letters. PMID 34156254 DOI: 10.1021/acs.orglett.1c01767 |
0.34 |
|
2021 |
Fan J, Wei Q, Zhu E, Gao J, Cheng X, Lu Y, Loh TP. Visible light-induced mono-bromination of arenes with BrCCl. Chemical Communications (Cambridge, England). PMID 34027541 DOI: 10.1039/d1cc01721g |
0.353 |
|
2021 |
Shi S, Yang X, Tang M, Hu J, Loh TP. Direct Synthesis of α-Amino Nitriles from Sulfonamides via Base-Mediated C-H Cyanation. Organic Letters. PMID 33970649 DOI: 10.1021/acs.orglett.1c01232 |
0.315 |
|
2021 |
Goh J, Maraswami M, Loh TP. Synthesis of Vinylic Sulfones in Aqueous Media. Organic Letters. 23: 1060-1065. PMID 33492146 DOI: 10.1021/acs.orglett.0c04257 |
0.376 |
|
2020 |
Pal KB, Guo A, Das M, Lee J, Báti G, Yip BRP, Loh TP, Liu XW. Iridium-promoted deoxyglycoside synthesis: stereoselectivity and mechanistic insight. Chemical Science. 12: 2209-2216. PMID 34163986 DOI: 10.1039/d0sc06529c |
0.369 |
|
2020 |
Maraswami M, Goh J, Loh TP. Macrolactam Synthesis via Ring-Closing Alkene-Alkene Cross-Coupling Reactions. Organic Letters. PMID 33258611 DOI: 10.1021/acs.orglett.0c03801 |
0.402 |
|
2020 |
Zhao K, Zhang ZY, Cui XL, Wang YX, Wu XD, Li WM, Wu JX, Zhao LL, Guo JY, Loh TP. Visible-Light-Induced Regio- and Stereoselective C(sp)-H Trifluoroethylation of Enamides with 2,2,2-Trifluoroethyl Iodide. Organic Letters. PMID 33176097 DOI: 10.1021/acs.orglett.0c03418 |
0.33 |
|
2020 |
Lu MZ, Luo H, Hu Z, Shao C, Kan Y, Loh TP. Directed Palladium(II)-Catalyzed Intermolecular Anti-Markovnikov Hydroarylation of Unactivated Alkenes with (Hetero)arylsilanes. Organic Letters. PMID 33151076 DOI: 10.1021/acs.orglett.0c03416 |
0.349 |
|
2020 |
Guo P, Sun W, Liu Y, Li YX, Loh TP, Jiang Y. Stereoselective Synthesis of Vinylcyclopropa[]indolines via a Rh-Migration Strategy. Organic Letters. PMID 32672043 DOI: 10.1021/Acs.Orglett.0C02071 |
0.429 |
|
2020 |
Xie P, Sun Z, Li S, Cai X, Qiu J, Fu W, Gao C, Wu S, Yang X, Loh TP. Reciprocal-Activation Strategy for Allylic Sulfination with Unactivated Allylic Alcohols. Organic Letters. PMID 32496788 DOI: 10.1021/acs.orglett.0c01747 |
0.38 |
|
2020 |
Lu MZ, Ding X, Shao C, Hu Z, Luo H, Zhi S, Hu H, Kan Y, Loh TP. Direct Hiyama Cross-Coupling of (Hetero)arylsilanes with C(sp)-H Bonds Enabled by Cobalt Catalysis. Organic Letters. PMID 32182081 DOI: 10.1021/Acs.Orglett.0C00631 |
0.393 |
|
2020 |
Chen Y, Yang W, Wu J, Sun W, Loh TP, Jiang Y. 2-Azirines as Potential Bifunctional Chemical Linkers of Cysteine Residues in Bioconjugate Technology. Organic Letters. PMID 32105086 DOI: 10.1021/Acs.Orglett.0C00415 |
0.398 |
|
2020 |
Liu RH, Shen ZY, Wang C, Loh TP, Hu XH. Selective Dehydrogenative Acylation of Enamides with Aldehydes Leading to Valuable β-Ketoenamides. Organic Letters. PMID 31971809 DOI: 10.1021/Acs.Orglett.9B04495 |
0.37 |
|
2020 |
Liang X, Guo P, Yang W, Li M, Jiang C, Sun W, Loh TP, Jiang Y. Stereoselective synthesis of trifluoromethyl-substituted 2H-furan-amines from enaminones. Chemical Communications (Cambridge, England). PMID 31967112 DOI: 10.1039/c9cc08582c |
0.375 |
|
2020 |
Zheng K, Xiao G, Guo T, Ding Y, Wang C, Loh TP, Wu X. Intermolecular Reductive Heck Reaction of Unactivated Aliphatic Alkenes with Organohalides. Organic Letters. PMID 31913642 DOI: 10.1021/Acs.Orglett.9B04474 |
0.531 |
|
2020 |
Zhao K, Zhang X, Tao J, Wu X, Wu J, Li W, Zhu T, Loh T. Regio- and stereoselective C(sp2)–H acylation of enamides with aldehydes via transition-metal-free photoredox catalysis Green Chemistry. 22: 5497-5503. DOI: 10.1039/D0Gc01947J |
0.359 |
|
2020 |
Guo T, Ding Y, Zhou L, Xu H, Loh T, Wu X. Palladium-Catalyzed anti-Michael Reductive Heck Reaction of α, β-unsaturated esters Acs Catalysis. 10: 7262-7268. DOI: 10.1021/Acscatal.0C02414 |
0.463 |
|
2020 |
Rong J, Li H, Fu R, Sun W, Loh T, Jiang Y. Cleavage and Reassembly C≡C Bonds of Ynones to Access Highly Functionalized Ketones Acs Catalysis. 10: 3664-3669. DOI: 10.1021/Acscatal.0C00381.S001 |
0.473 |
|
2019 |
Guo JY, Zhang ZY, Guan T, Mao LW, Ban Q, Zhao K, Loh TP. Photoredox-catalyzed stereoselective alkylation of enamides with -hydroxyphthalimide esters decarboxylative cross-coupling reactions. Chemical Science. 10: 8792-8798. PMID 31803451 DOI: 10.1039/c9sc03070k |
0.394 |
|
2019 |
Guo JY, Guan T, Tao JY, Zhao K, Loh TP. Stereoselective C(sp)-H Alkylation of Enamides with Unactivated Aliphatic Carboxylic Acids via Decarboxylative Cross-Coupling Reactions. Organic Letters. PMID 31580083 DOI: 10.1021/Acs.Orglett.9B03169 |
0.498 |
|
2019 |
Xu Y, Liu ZL, Yang C, Xue QY, Zhao M, Shan CC, Loh TP. Copper-catalyzed Asymmetric Silylation of Propargyl Dichlorides: Access to Enantioenriched Functionalized Allenylsilanes. Angewandte Chemie (International Ed. in English). PMID 31532868 DOI: 10.1002/Anie.201908343 |
0.464 |
|
2019 |
Shi P, Li S, Hu LM, Wang C, Loh TP, Hu XH. The ruthenium-catalyzed C-H functionalization of enamides with isocyanates: easy entry to pyrimidin-4-ones. Chemical Communications (Cambridge, England). PMID 31461097 DOI: 10.1039/C9Cc03612A |
0.392 |
|
2019 |
Xie P, Fu W, Cai X, Sun Z, Wu Y, Li S, Gao C, Yang X, Loh TP. A Ba/Pd Catalytic System Enables Dehydrative Cross-Coupling and Excellent -Selective Wittig Reactions. Organic Letters. PMID 31430163 DOI: 10.1021/acs.orglett.9b02623 |
0.324 |
|
2019 |
Li SS, Zhao M, Liu XW, Xu JL, Xu YH, Loh TP. Palladium-Catalyzed Cycloaromatization/Alkylation of o-(Alkynyl)styrenes. The Journal of Organic Chemistry. PMID 31414808 DOI: 10.1021/Acs.Joc.9B01630 |
0.489 |
|
2019 |
Liu DY, Zhu SM, Li RQ, Tian JS, Loh TP. α-Amino Acetal: A Synthetic Intermediate for the Construction of Aza-Polycycles. Organic Letters. PMID 31369288 DOI: 10.1021/Acs.Orglett.9B02240 |
0.396 |
|
2019 |
Zhu TH, Zhang ZY, Tao JY, Zhao K, Loh TP. Regioselective and Stereoselective Difluoromethylation of Enamides with Difluoromethyltriphenylphosphonium Bromide via Photoredox Catalysis. Organic Letters. PMID 31339728 DOI: 10.1021/Acs.Orglett.9B02361 |
0.444 |
|
2019 |
Liu XY, Li XR, Zhang C, Chu XQ, Rao W, Loh TP, Shen ZL. Iron(0)-Mediated Reformatsky Reaction for the Synthesis of β-Hydroxyl Carbonyl Compounds. Organic Letters. PMID 31318222 DOI: 10.1021/Acs.Orglett.9B01999 |
0.469 |
|
2019 |
Chen J, Guo P, Zhang J, Rong J, Sun W, Jiang Y, Loh TP. Catalytic Synthesis of Functionalized α-Vinyl Aldehydes from Enaminones. Angewandte Chemie (International Ed. in English). PMID 31278817 DOI: 10.1002/Anie.201906213 |
0.503 |
|
2019 |
Zhang YH, Zhang WW, Zhang ZY, Zhao K, Loh TP. Manganese-Catalyzed Ring-Opening Coupling Reactions of Cyclopropanols with Enones. Organic Letters. PMID 31247809 DOI: 10.1021/Acs.Orglett.9B01703 |
0.494 |
|
2019 |
Ahmad T, Li Q, Qiu SQ, Xu JL, Xu YH, Loh TP. Copper-catalyzed regiodivergent 1,4- and 1,6-conjugate silyl addition to diendioates: access to functionalized allylsilanes. Organic & Biomolecular Chemistry. PMID 31172157 DOI: 10.1039/C9Ob01086F |
0.483 |
|
2019 |
Qiu SQ, Ahmad T, Xu YH, Loh TP. Palladium-Catalyzed Cascade Intramolecular Cyclization and Allylation of Enynoates with Allylic Alcohols. The Journal of Organic Chemistry. PMID 31081618 DOI: 10.1021/Acs.Joc.9B00461 |
0.494 |
|
2019 |
Liu XW, Li SS, Dai DT, Zhao M, Shan CC, Xu YH, Loh TP. Palladium-Catalyzed Dialkylation of C-C Triple Bonds: Access to Multi-Functionalized Indenes. Organic Letters. PMID 31070377 DOI: 10.1021/Acs.Orglett.9B01163 |
0.506 |
|
2019 |
Liu RH, Shan QC, Hu XH, Loh TP. Site-selective C(sp)-H amination of thioamide with anthranils under Cp*Co catalysis. Chemical Communications (Cambridge, England). PMID 31020280 DOI: 10.1039/C9Cc01715A |
0.334 |
|
2019 |
Cheng BQ, Zhao SW, Song XD, Chu XQ, Rao W, Loh TP, Shen ZL. Lead-Mediated Highly Diastereoselective Allylation of Aldehydes with Cyclic Allylic Halides. The Journal of Organic Chemistry. PMID 30977647 DOI: 10.1021/Acs.Joc.9B00370 |
0.498 |
|
2019 |
Meng FF, Xue QY, Jiang B, Zhao M, Xie JH, Xu YH, Loh TP. Divergent Protosilylation and Protoborylation of Polar Enynes. Organic Letters. PMID 30939022 DOI: 10.1021/Acs.Orglett.9B00995 |
0.357 |
|
2019 |
Ding Y, Zhang SY, Chen YC, Fan SX, Tian JS, Loh TP. Regioselective C-H Amidation of (Alkyl)arenes by Iron(II) Catalysis. Organic Letters. PMID 30920841 DOI: 10.1021/Acs.Orglett.9B00697 |
0.454 |
|
2019 |
Li S, Shi P, Liu RH, Hu XH, Loh TP. Cobalt-Catalyzed N-O and C-C Bond Cleavage in 1,2-Oxazetidines: Solvent-Controlled C-H Aminomethylation and Hydroxymethylation of Heteroarenes. Organic Letters. PMID 30807182 DOI: 10.1021/Acs.Orglett.9B00141 |
0.362 |
|
2019 |
Tian MQ, Wang C, Hu XH, Loh TP. Divergent C-H Oxidative Radical Functionalization of Olefins to Install Tertiary Alkyl Motifs Enabled by Copper Catalysis. Organic Letters. PMID 30793908 DOI: 10.1021/Acs.Orglett.9B00142 |
0.501 |
|
2019 |
Zhi ML, Chen BZ, Deng W, Chu XQ, Loh TP, Shen ZL. Preparation of Alkyl Indium Reagents by Iodine-Catalyzed Direct Indium Insertion and Their Applications in Cross-Coupling Reactions. The Journal of Organic Chemistry. PMID 30721056 DOI: 10.1021/Acs.Joc.9B00204 |
0.501 |
|
2019 |
Ge Y, Sun W, Chen Y, Huang Y, Liu Z, Jiang Y, Loh TP. Reactions of 5-Aminoisoxazoles with α-Diazocarbonyl Compounds: Wolff Rearrangement vs N-H Insertion. The Journal of Organic Chemistry. PMID 30702883 DOI: 10.1021/Acs.Joc.8B02986 |
0.46 |
|
2019 |
Maraswami M, Loh T. Transition-Metal-Catalyzed Alkenyl sp2 C–H Activation: A Short Account Synthesis. 51: 1049-1062. DOI: 10.1055/S-0037-1611649 |
0.346 |
|
2019 |
Li M, Bao C, Liu Y, Meng J, Liu X, Cai Y, Wuu D, Zong Y, Loh T, Wang Z. Reduced graphene oxide-supported cobalt oxide decorated N-doped graphitic carbon for efficient bifunctional oxygen electrocatalysis Rsc Advances. 9: 16534-16540. DOI: 10.1039/C9Ra02389E |
0.303 |
|
2019 |
He G, Li Y, Yu Z, Chen Z, Tang Y, Song G, Loh T. Selectfluor™-catalyzed oxidative cyclization of ynamides enables facile synthesis of oxazolidine-2,4-diones Organic Chemistry Frontiers. 6: 3644-3648. DOI: 10.1039/C9Qo00845D |
0.394 |
|
2019 |
Chu X, Ge D, Loh T, Shen Z. Oxidant-directed chemoselective sulfonylation and sulfonyloximation of alkenes via cleaving the C–S bond in TosMIC Organic Chemistry Frontiers. 6: 835-840. DOI: 10.1039/C8Qo01346B |
0.433 |
|
2019 |
Zhu T, Zhang X, Zhao K, Loh T. Cu(OTf)2-mediated C(sp2)–H arylsulfonylation of enamides via the insertion of sulfur dioxide Organic Chemistry Frontiers. 6: 94-98. DOI: 10.1039/C8Qo01144C |
0.435 |
|
2019 |
Qiang W, Liu X, Loh T. Supported Iridium Catalyst for the Green Synthesis of 3,3′-Bis(indolyl)methanes Using Methanol As the Bridging Methylene Source Acs Sustainable Chemistry & Engineering. 7: 8429-8439. DOI: 10.1021/Acssuschemeng.9B00094 |
0.437 |
|
2019 |
Shen Z, Cheng J, Wang C, Yuan C, Loh T, Hu X. Iron-Catalyzed Carbamoylation of Enamides with Formamides as a Direct Approach to N-Acyl Enamine Amides Acs Catalysis. 9: 8128-8135. DOI: 10.1021/Acscatal.9B02635 |
0.359 |
|
2019 |
Luo Y, Yang C, Qiu S, Liang Q, Xu Y, Loh T. Palladium(II)-Catalyzed Stereospecific Alkenyl C–H Bond Alkylation of Allylamines with Alkyl Iodides Acs Catalysis. 9: 4271-4276. DOI: 10.1021/Acscatal.8B04415 |
0.446 |
|
2019 |
Bao C, Liu X, Li M, Meng J, Cai Y, Huang X, Loh T, Wang Z. MoS2-nanosheet-decorated C-N/Co4S3 nanorod hybrid as a bifunctional electrocatalyst Electrochemistry Communications. 106: 106515. DOI: 10.1016/J.Elecom.2019.106515 |
0.349 |
|
2019 |
Chu X, Shen Z, Loh T. Regioselective (Hetero)aryl C–H Thianthrenation and Late-Stage Transformations Chem. 5: 1025-1027. DOI: 10.1016/J.Chempr.2019.04.011 |
0.336 |
|
2019 |
Song S, Liu H, Wang L, Zhu C, Loh T, Feng C. Rhodium‐Catalyzed Defluorinative Vinylation of gem‐Difluoroalkenes for the Synthesis of 2‐Fluoro‐1,3‐dienes Chinese Journal of Chemistry. 37: 1036-1040. DOI: 10.1002/Cjoc.201900197 |
0.418 |
|
2019 |
Chu X, Ge D, Wang M, Rao W, Loh T, Shen Z. Chemo‐ and Regioselective Ring Construction Driven by Visible‐Light Photoredox Catalysis: an Access to Fluoroalkylated Oxazolidines Featuring an All‐Substituted Carbon Stereocenter Advanced Synthesis & Catalysis. 361: 4082-4090. DOI: 10.1002/Adsc.201900585 |
0.3 |
|
2019 |
Hu J, Cheng B, Yang X, Loh T. Transition‐Metal‐Free Deaminative Vinylation of Alkylamines Advanced Synthesis & Catalysis. 361: 4902-4908. DOI: 10.1002/Adsc.201900576 |
0.403 |
|
2019 |
Liu X, Cheng B, Guo Y, Chu X, Li Y, Loh T, Shen Z. Bismuth‐Mediated Diastereoselective Allylation Reaction of Carbonyl Compounds with Cyclic Allylic Halides or Cinnamyl Halide Advanced Synthesis & Catalysis. 361: 542-549. DOI: 10.1002/Adsc.201801297 |
0.472 |
|
2018 |
Liang G, Rong J, Sun W, Chen G, Jiang Y, Loh TP. Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization. Organic Letters. PMID 30403359 DOI: 10.1021/Acs.Orglett.8B03284 |
0.464 |
|
2018 |
Ahmad T, Qiu SQ, Xu YH, Loh TP. Palladium-Catalyzed One-Pot Highly Regioselective 6- Endo Cyclization and Alkylation of Enynoates: Synthesis of 2-Alkanone Pyrones. The Journal of Organic Chemistry. PMID 30354107 DOI: 10.1021/Acs.Joc.8B02198 |
0.465 |
|
2018 |
Wo X, Xie P, Fu W, Gao C, Liu Y, Sun Z, Loh TP. Barium-catalyzed C-OH/P-H dehydrative cross-coupling for C-P bond construction. Chemical Communications (Cambridge, England). PMID 30225501 DOI: 10.1039/C8Cc06530F |
0.371 |
|
2018 |
Yun JJ, Liu XY, Deng W, Chu XQ, Shen ZL, Loh TP. Chromium(III)-Catalyzed Addition of Water and Alcohol to α,β-Unsaturated Ketones for The Synthesis of β-Hydroxyl and β-Alkoxyl Ketones in Aqueous Media. The Journal of Organic Chemistry. PMID 30110165 DOI: 10.1021/Acs.Joc.8B01584 |
0.4 |
|
2018 |
Liu Y, Xie P, Sun Z, Wo X, Gao C, Fu W, Loh TP. Direct Substitution of Secondary and Tertiary Alcohols To Generate Sulfones under Catalyst- and Additive-Free Conditions. Organic Letters. PMID 30106300 DOI: 10.1021/Acs.Orglett.8B02188 |
0.432 |
|
2018 |
Wang C, Liu RH, Tian MQ, Hu XH, Loh TP. Regioselective Copper-Catalyzed Oxidative Coupling of α-Alkylated Styrenes with Tertiary Alkyl Radicals. Organic Letters. PMID 29943570 DOI: 10.1021/Acs.Orglett.8B01600 |
0.41 |
|
2018 |
Wang C, Xiao G, Guo T, Ding Y, Wu X, Loh TP. Palladium-Catalyzed Regiocontrollable Reductive Heck Reaction of Unactivated Aliphatic Alkenes. Journal of the American Chemical Society. PMID 29925236 DOI: 10.1021/Jacs.8B03619 |
0.511 |
|
2018 |
Liang QJ, Jiang B, Xu YH, Loh TP. Palladium-Catalyzed Regioselective Olefination of O-Acetyl Cyanohydrins. The Journal of Organic Chemistry. PMID 29902382 DOI: 10.1021/Acs.Joc.8B00991 |
0.39 |
|
2018 |
Zhou S, Yan BW, Fan SX, Tian JS, Loh TP. Regioselective Formal [4 + 2] Cycloadditions of Enaminones with Diazocarbonyls through Rh-Catalyzed C-H Bond Functionalization. Organic Letters. PMID 29888603 DOI: 10.1021/Acs.Orglett.8B01540 |
0.482 |
|
2018 |
Jiang B, Liang QJ, Han Y, Zhao M, Xu YH, Loh TP. Copper-Catalyzed Dehydrogenative Diels-Alder Reaction. Organic Letters. PMID 29790760 DOI: 10.1021/Acs.Orglett.8B01067 |
0.492 |
|
2018 |
Xie P, Fan J, Liu Y, Wo X, Fu W, Loh TP. Bronsted Acid/Organic Photoredox Cooperative Catalysis: Easy Access to Tri- and Tetrasubstituted Alkenylphosphorus Compounds from Alcohols and P-H Species. Organic Letters. PMID 29781271 DOI: 10.1021/Acs.Orglett.8B01173 |
0.357 |
|
2018 |
Zhou L, Zhu C, Loh TP, Feng C. Rh-Catalyzed C-H bond alkylation of indoles with α,α-difluorovinyl tosylate via indolyl group migration. Chemical Communications (Cambridge, England). PMID 29770372 DOI: 10.1039/C8Cc02183J |
0.366 |
|
2018 |
Ge Y, Sun W, Pei B, Ding J, Jiang Y, Loh TP. Hoveyda-Grubbs II Catalyst: A Useful Catalyst for One-Pot Visible-Light-Promoted Ring Contraction and Olefin Metathesis Reactions. Organic Letters. PMID 29693396 DOI: 10.1021/Acs.Orglett.8B00971 |
0.406 |
|
2018 |
Zhang QC, Zhang WW, Shen L, Shen ZL, Loh TP. In(III)-TMSBr-Catalyzed Cascade Reaction of Diarylalkynes with Acrylates for the Synthesis of Aryldihydronaphthalene Derivatives. Molecules (Basel, Switzerland). 23. PMID 29690598 DOI: 10.3390/Molecules23040979 |
0.472 |
|
2018 |
Chu XQ, Xie T, Li L, Ge D, Shen ZL, Loh TP. Combining Fluoroalkylation and Defluorination to Enable Formal [3 + 2 + 1] Heteroannulation by Using Visible-Light Photoredox Organocatalysis. Organic Letters. PMID 29683679 DOI: 10.1021/Acs.Orglett.8B00963 |
0.33 |
|
2018 |
Xie P, Wang J, Liu Y, Fan J, Wo X, Fu W, Sun Z, Loh TP. Water-promoted C-S bond formation reactions. Nature Communications. 9: 1321. PMID 29615622 DOI: 10.1038/S41467-018-03698-8 |
0.444 |
|
2018 |
Chen BZ, Zhi ML, Wang CX, Chu XQ, Shen ZL, Loh TP. Synthesis of Alkyl Indium Reagents by Using Unactivated Alkyl Chlorides and Their Applications in Palladium-Catalyzed Cross-Coupling Reactions with Aryl Halides. Organic Letters. PMID 29527900 DOI: 10.1021/Acs.Orglett.8B00441 |
0.511 |
|
2018 |
Li RQ, He Y, Ding Y, Ang CK, Tian JS, Loh TP. Formal synthesis of chelamidine alkaloids and their derivatives. Chemical Communications (Cambridge, England). PMID 29527613 DOI: 10.1039/c7cc09875h |
0.416 |
|
2018 |
Chu XQ, Cheng BQ, Zhang YW, Ge D, Shen ZL, Loh TP. Copper-catalyzed three-component cyclization of amidines, styrenes, and fluoroalkyl halides for the synthesis of modular fluoroalkylated pyrimidines. Chemical Communications (Cambridge, England). PMID 29479589 DOI: 10.1039/c7cc09571f |
0.319 |
|
2018 |
Zhang Q, Liang QJ, Xu JL, Xu YH, Loh TP. Palladium-catalyzed silaborative carbocyclizations of 1,6-diynes. Chemical Communications (Cambridge, England). PMID 29450429 DOI: 10.1039/c8cc00097b |
0.426 |
|
2018 |
Wang F, Sun W, Wang Y, Jiang Y, Loh TP. Highly Site-Selective Metal-Free C-H Acyloxylation of Stable Enamines. Organic Letters. PMID 29419306 DOI: 10.1021/Acs.Orglett.8B00222 |
0.395 |
|
2018 |
Jiang Y, Deng G, Zhang S, Loh TP. Directing Group Participated Benzylic C(sp3)-H/C(sp2)-H Cross-Dehydrogenative Coupling (CDC): Synthesis of Azapolycycles. Organic Letters. PMID 29328666 DOI: 10.1021/Acs.Orglett.7B03748 |
0.393 |
|
2018 |
Da B, Liang Q, Luo Y, Ahmad T, Xu Y, Loh T. Copper-Catalyzed Stereo- and Enantioselective 1,4-Protosilylation of α,β-Unsaturated Ketimines To Synthesize Functionalized Allylsilanes Acs Catalysis. 8: 6239-6245. DOI: 10.1021/Acscatal.8B01547 |
0.46 |
|
2018 |
Meng F, Xie J, Xu Y, Loh T. Catalytically Asymmetric Synthesis of 1,3-Bis(silyl)propenes via Copper-Catalyzed Double Proto-Silylations of Polar Enynes Acs Catalysis. 8: 5306-5312. DOI: 10.1021/Acscatal.8B00999 |
0.518 |
|
2018 |
Chu X, Ge D, Shen Z, Loh T. Recent Advances in Radical-Initiated C(sp3)–H Bond Oxidative Functionalization of Alkyl Nitriles Acs Catalysis. 8: 258-271. DOI: 10.1021/Acscatal.7B03334 |
0.393 |
|
2018 |
Deng G, Chen J, Sun W, Bian K, Jiang Y, Loh T. Bioinspired Deamination of α
-Amino Acid Derivatives Catalyzed by a Palladium/Nickel Complex Advanced Synthesis & Catalysis. 360: 3900-3905. DOI: 10.1002/Adsc.201800823 |
0.375 |
|
2018 |
Yun J, Zhi M, Shi W, Chu X, Shen Z, Loh T. Indium(III)‐Catalyzed Hydration and Hydroalkoxylation of α,β‐Unsaturated Ketones in Aqueous Media Advanced Synthesis & Catalysis. 360: 2632-2637. DOI: 10.1002/Adsc.201800301 |
0.313 |
|
2018 |
Cai S, Wang D, Ye L, Liu Z, Feng C, Loh T. Pyrroline Synthesis via Visible‐Light‐Promoted Hydroimination of Unactivated Alkenes with N,N′‐Dimethylpropylene Urea as H‐Donor Advanced Synthesis & Catalysis. 360: 1262-1266. DOI: 10.1002/Adsc.201700937 |
0.346 |
|
2018 |
Maraswami M, Chen G, Loh T. Iridium(III)‐Catalyzed Selective and Mild C‐H Amidation of Cyclic N‐Sulfonyl Ketimines with Organic Azides Advanced Synthesis & Catalysis. 360: 416-421. DOI: 10.1002/Adsc.201700785 |
0.479 |
|
2017 |
Jiang B, Zhao M, Li SS, Xu YH, Loh TP. Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes. Angewandte Chemie (International Ed. in English). PMID 29193496 DOI: 10.1002/Anie.201710601 |
0.464 |
|
2017 |
Cheng JK, Shen L, Wu LH, Hu XH, Loh TP. Iron-catalyzed peroxidation-carbamoylation of alkenes with hydroperoxides and formamides via formyl C(sp(2))-H functionalization. Chemical Communications (Cambridge, England). PMID 29143011 DOI: 10.1039/C7Cc08074C |
0.411 |
|
2017 |
Ye L, Cai SH, Wang DX, Wang YQ, Lai LJ, Feng C, Loh TP. Photoredox Catalysis Induced Bisindolylation of Ethers/Alcohols via Sequential C-H and C-O Bond Cleavage. Organic Letters. PMID 29112428 DOI: 10.1021/Acs.Orglett.7B03073 |
0.363 |
|
2017 |
Lan Y, Fan P, Liu XW, Meng FF, Ahmad T, Xu YH, Loh TP. An iron-catalyzed hydroalkylation reaction of α,β-unsaturated ketones with ethers. Chemical Communications (Cambridge, England). PMID 29099147 DOI: 10.1039/C7Cc07235J |
0.446 |
|
2017 |
Ni M, Zhang J, Liang X, Jiang Y, Loh TP. Directed C-C bond cleavage of a cyclopropane intermediate generated from N-tosylhydrazones and stable enaminones: expedient synthesis of functionalized 1,4-ketoaldehydes. Chemical Communications (Cambridge, England). PMID 29094130 DOI: 10.1039/C7Cc07178G |
0.387 |
|
2017 |
Shen L, Zhao K, Doitomi K, Ganguly R, Li Y, Shen ZL, Hirao H, Loh TP. Lewis Acid-catalyzed Selective [2+2]-Cycloaddition and Dearomatizing Cascade Reaction of Aryl Alkynes with Acrylates. Journal of the American Chemical Society. PMID 28880536 DOI: 10.1021/Jacs.7B07997 |
0.511 |
|
2017 |
Zhu C, Song S, Zhou L, Wang DX, Feng C, Loh TP. Nonconventional difluoroalkylation of C(sp(2))-H bonds through hydroarylation. Chemical Communications (Cambridge, England). PMID 28795700 DOI: 10.1039/C7Cc04842D |
0.417 |
|
2017 |
Chang XH, Liu ZL, Luo YC, Yang C, Liu XW, Da BC, Li JJ, Ahmad T, Loh TP, Xu YH. Copper-catalyzed silylation reactions of propargyl epoxides: easy access to 2,3-allenols and stereodefined alkenes. Chemical Communications (Cambridge, England). PMID 28783200 DOI: 10.1039/c7cc04588c |
0.433 |
|
2017 |
Maraswami M, Pankajakshan S, Chen G, Loh TP. Palladium-Catalyzed Direct C-H Trifluoroethylation of Aromatic Amides. Organic Letters. PMID 28782962 DOI: 10.1021/Acs.Orglett.7B01859 |
0.304 |
|
2017 |
Cai SH, Ye L, Wang DX, Wang YQ, Lai LJ, Zhu C, Feng C, Loh TP. Manganese-catalyzed synthesis of monofluoroalkenes via C-H activation and C-F cleavage. Chemical Communications (Cambridge, England). PMID 28726856 DOI: 10.1039/C7Cc04131D |
0.381 |
|
2017 |
Tang HJ, Lin LZ, Feng C, Loh TP. Palladium-Catalyzed Fluoroarylation of gem-Difluoroalkenes. Angewandte Chemie (International Ed. in English). PMID 28646533 DOI: 10.1002/Anie.201705321 |
0.401 |
|
2017 |
Song S, Lu P, Liu H, Cai SH, Feng C, Loh TP. Switchable C-H Functionalization of N-Tosyl Acrylamides with Acryloylsilanes. Organic Letters. PMID 28534624 DOI: 10.1021/Acs.Orglett.7B01107 |
0.457 |
|
2017 |
Liang QJ, Yang C, Meng FF, Jiang B, Xu YH, Loh TP. Chelation versus Non-Chelation Control in the Stereoselective Alkenyl sp(2) C-H Bond Functionalization Reaction. Angewandte Chemie (International Ed. in English). PMID 28370972 DOI: 10.1002/Anie.201700559 |
0.485 |
|
2017 |
Jiang B, Meng FF, Liang QJ, Xu YH, Loh TP. Palladium-Catalyzed Direct Intramolecular C-N Bond Formation: Access to Multisubstituted Dihydropyrroles. Organic Letters. PMID 28181813 DOI: 10.1021/Acs.Orglett.7B00072 |
0.503 |
|
2017 |
Wang CQ, Ye L, Feng C, Loh TP. C-F Bond Cleavage Enabled Redox-Neutral [4+1] Annulation via C-H Bond Activation. Journal of the American Chemical Society. PMID 28098988 DOI: 10.1021/Jacs.6B12142 |
0.43 |
|
2017 |
Lan Y, Yang C, Xu Y, Loh T. Direct coupling of sp3 carbon of alkanes with α,β-unsaturated carbonyl compounds using a copper/hydroperoxide system Organic Chemistry Frontiers. 4: 1411-1415. DOI: 10.1039/C7Qo00149E |
0.376 |
|
2017 |
Lu M, Wang C, Song S, Loh T. Rhodium(III)-catalyzed directed C–H benzylation and allylation of indoles with organosilicon reagents Organic Chemistry Frontiers. 4: 303-307. DOI: 10.1039/C6Qo00589F |
0.445 |
|
2017 |
Lan Y, Chang X, Fan P, Shan C, Liu Z, Loh T, Xu Y. Copper-Catalyzed Silylperoxidation Reaction of α,β-Unsaturated Ketones, Esters, Amides, and Conjugated Enynes Acs Catalysis. 7: 7120-7125. DOI: 10.1021/Acscatal.7B02754 |
0.435 |
|
2016 |
Liu H, Song S, Wang CQ, Feng C, Loh TP. Redox-Neutral Rhodium-Catalyzed [4+1] Annulation through Formal Dehydrogenative Vinylidene Insertion. Chemsuschem. PMID 27976532 DOI: 10.1002/Cssc.201601341 |
0.471 |
|
2016 |
Tian P, Wang CQ, Cai SH, Song S, Ye L, Feng C, Loh TP. F(-) Nucleophilic-Addition-Induced Allylic Alkylation. Journal of the American Chemical Society. 138: 15869-15872. PMID 27960318 DOI: 10.1021/Jacs.6B11205 |
0.466 |
|
2016 |
Zhao K, Shen L, Shen ZL, Loh TP. Transition metal-catalyzed cross-coupling reactions using organoindium reagents. Chemical Society Reviews. PMID 27827485 DOI: 10.1039/C6Cs00465B |
0.41 |
|
2016 |
Ren S, Song S, Ye L, Feng C, Loh TP. Copper-catalyzed oxyamination of electron-deficient alkenes with N-acyloxyamines. Chemical Communications (Cambridge, England). PMID 27481485 DOI: 10.1039/C6Cc04638J |
0.407 |
|
2016 |
Zhou JH, Cai SH, Xu YH, Loh TP. Anomalous Reactivity and Selectivity in the Intermolecular Diels-Alder Reactions of Multisubstituted Acyclic Dienes with Geometrical Isomers of Enals. Organic Letters. PMID 27132468 DOI: 10.1021/acs.orglett.6b00783 |
0.323 |
|
2016 |
Ding R, Huang ZD, Liu ZL, Wang TX, Xu YH, Loh TP. Palladium-catalyzed cross-coupling of enamides with sterically hindered α-bromocarbonyls. Chemical Communications (Cambridge, England). PMID 27029562 DOI: 10.1039/c5cc10653b |
0.377 |
|
2016 |
Huang ZD, Ding R, Wang P, Xu YH, Loh TP. Palladium-catalyzed silylation reaction between benzylic halides and silylboronate. Chemical Communications (Cambridge, England). PMID 27026113 DOI: 10.1039/c6cc00713a |
0.396 |
|
2016 |
Hu X, Yang X, Loh T. Chelation-Assisted Rhodium-Catalyzed Direct Amidation with Amidobenziodoxolones: C(sp2)–H, C(sp3)–H, and Late-Stage Functionalizations Acs Catalysis. 6: 5930-5934. DOI: 10.1021/Acscatal.6B02015 |
0.373 |
|
2016 |
Cai SH, Xie JH, Song S, Ye L, Feng C, Loh TP. Visible-light-promoted carboimination of unactivated alkenes for the synthesis of densely functionalized pyrroline derivatives Acs Catalysis. 6: 5571-5574. DOI: 10.1021/Acscatal.6B01230 |
0.429 |
|
2016 |
Cai S, Da B, Zhou J, Xu Y, Loh T. Stereoselective Synthesis of cis‐2,5‐Disubstituted Pyrrolidines via Copper‐Catalyzed Cyclization of Alkenes Chinese Journal of Chemistry. 34: 1076-1080. DOI: 10.1002/Cjoc.201600380 |
0.454 |
|
2016 |
Wang CQ, Feng C, Loh TP. RhIII-Catalyzed Hydroarylation of Internal Alkynes through C−H Bond Activation Asian Journal of Organic Chemistry. 5: 1002-1007. DOI: 10.1002/Ajoc.201600144 |
0.43 |
|
2015 |
Liu YY, Lin JY, Bo YF, Xie LH, Yi MD, Zhang XW, Zhang HM, Loh TP, Huang W. Synthesis and Crystal Structure of Highly Strained [4]Cyclofluorene: Green-Emitting Fluorophore. Organic Letters. PMID 26695881 DOI: 10.1021/Acs.Orglett.5B03038 |
0.498 |
|
2015 |
Wang M, Liu ZL, Zhang X, Tian PP, Xu YH, Loh TP. Synthesis of Highly Substituted Racemic and Chiral Allenylsilanes via Copper-Catalyzed Hydrosilylation of (Z)-2-Alken-4-ynoates with Silylboronate. Journal of the American Chemical Society. PMID 26560851 DOI: 10.1021/Jacs.5B08279 |
0.537 |
|
2015 |
Hu XH, Yang XF, Loh TP. Selective Alkenylation and Hydroalkenylation of Enol Phosphates through Direct CH Functionalization. Angewandte Chemie (International Ed. in English). PMID 26530687 DOI: 10.1002/Anie.201506437 |
0.428 |
|
2015 |
Liu J, Tan CH, Loh TP, Badrick T. A simple approach to derive Z-score of reference change value involving more than two serial results. Annals of Clinical Biochemistry. 52: 717-9. PMID 26483563 DOI: 10.1177/0004563215595430 |
0.402 |
|
2015 |
Liu J, Tan CH, Loh TP, Badrick T. Detecting Long-term Drift in Reagent Lots. Clinical Chemistry. 61: 1292-8. PMID 26272234 DOI: 10.1373/clinchem.2015.242511 |
0.38 |
|
2015 |
Qiu SQ, Xu YH, Loh TP. Palladium-Catalyzed Intermolecular Oxyarylation of Vinylacetates with Retention of an Alkenyl Moiety. Organic Letters. PMID 26135214 DOI: 10.1021/acs.orglett.5b01507 |
0.415 |
|
2015 |
Lu P, Feng C, Loh TP. Divergent Functionalization of Indoles with Acryloyl Silanes via Rhodium-Catalyzed C-H Activation. Organic Letters. PMID 26102089 DOI: 10.1021/acs.orglett.5b01258 |
0.391 |
|
2015 |
Tian P, Feng C, Loh TP. Rhodium-catalysed C(sp(2))-C(sp(2)) bond formation via C-H/C-F activation. Nature Communications. 6: 7472. PMID 26081837 DOI: 10.1038/Ncomms8472 |
0.376 |
|
2015 |
Chen YC, Zhu MK, Loh TP. Csp(3)-csp(3) bond cleavage in the palladium-catalyzed aminohydroxylation of allylic hydrazones using atmospheric oxygen as the sole oxidant. Organic Letters. 17: 2712-5. PMID 25973749 DOI: 10.1021/Acs.Orglett.5B01127 |
0.392 |
|
2015 |
Zhang X, Wang M, Ding R, Xu YH, Loh TP. Highly enantioselective and anti-diastereoselective catalytic intermolecular glyoxylate-ene reactions: effect of the geometrical isomers of alkenes. Organic Letters. 17: 2736-9. PMID 25965690 DOI: 10.1021/Acs.Orglett.5B01151 |
0.431 |
|
2015 |
Tian PP, Cai SH, Liang QJ, Zhou XY, Xu YH, Loh TP. Palladium-catalyzed difunctionalization of internal alkynes via highly regioselective 6-endo cyclization and alkenylation of enynoates: synthesis of multisubstituted pyrones. Organic Letters. 17: 1636-9. PMID 25789819 DOI: 10.1021/acs.orglett.5b00272 |
0.431 |
|
2015 |
Zhang S, Li L, Hu Y, Zha Z, Wang Z, Loh TP. Bifunctional amino sulfonohydrazide catalyzed direct asymmetric Mannich reaction of cyclic ketimines with ketones: highly diastereo- and enantioselective construction of quaternary carbon stereocenters. Organic Letters. 17: 1050-3. PMID 25664888 DOI: 10.1021/acs.orglett.5b00196 |
0.428 |
|
2015 |
Zhang LY, Zhou JH, Xu YH, Loh TP. Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate: synthesis of enantioenriched trifluoromethylated compounds. Chemistry, An Asian Journal. 10: 844-8. PMID 25655762 DOI: 10.1002/asia.201403303 |
0.307 |
|
2015 |
Hu XH, Zhang J, Yang XF, Xu YH, Loh TP. Stereo- and chemoselective cross-coupling between two electron-deficient acrylates: an efficient route to (Z,E)-muconate derivatives. Journal of the American Chemical Society. 137: 3169-72. PMID 25634134 DOI: 10.1021/ja512237d |
0.327 |
|
2015 |
Yang XF, Hu XH, Feng C, Loh TP. Rhodium(III)-catalyzed C7-position C-H alkenylation and alkynylation of indolines. Chemical Communications (Cambridge, England). 51: 2532-5. PMID 25567368 DOI: 10.1039/C4Cc09330E |
0.365 |
|
2015 |
Wang M, Zhang X, Zhuang YX, Xu YH, Loh TP. Pd-catalyzed intramolecular C-N bond cleavage, 1,4-migration, sp3 C-H activation, and Heck reaction: four controllable diverse pathways depending on the judicious choice of the base and ligand. Journal of the American Chemical Society. 137: 1341-7. PMID 25545361 DOI: 10.1021/Ja512212X |
0.373 |
|
2015 |
Feng C, Feng D, Loh TP. Rhodium(iii)-catalyzed C-H allylation of electron-deficient alkenes with allyl acetates. Chemical Communications (Cambridge, England). 51: 342-5. PMID 25406546 DOI: 10.1039/c4cc07597h |
0.365 |
|
2015 |
Zhang X, Wang M, Ding R, Xu YH, Loh TP. Highly enantioselective and anti -diastereoselective catalytic intermolecular glyoxylate-ene reactions: Effect of the geometrical isomers of alkenes Organic Letters. 17: 2736-2739. DOI: 10.1021/acs.orglett.5b01151 |
0.379 |
|
2015 |
Zhang S, Li L, Hu Y, Zha Z, Wang Z, Loh TP. Bifunctional amino sulfonohydrazide catalyzed direct asymmetric mannich reaction of cyclic ketimines with ketones: Highly diastereo-and enantioselective construction of quaternary carbon stereocenters Organic Letters. 17: 1050-1053. DOI: 10.1021/acs.orglett.5b00196 |
0.381 |
|
2015 |
Zhang LY, Zhou JH, Xu YH, Loh TP. Copper-Catalyzed Enantioselective Conjugate Addition of Grignard Reagents to Methyl 4,4,4-Trifluorocrotonate: Synthesis of Enantioenriched Trifluoromethylated Compounds Chemistry - An Asian Journal. DOI: 10.1002/asia.201403303 |
0.307 |
|
2014 |
Feng C, Feng D, Luo Y, Loh TP. Rhodium(III)-catalyzed olefinic C-H alkynylation of acrylamides using tosyl-imide as directing group. Organic Letters. 16: 5956-9. PMID 25383914 DOI: 10.1021/ol502984g |
0.301 |
|
2014 |
Tan CH, Han G, Loh TP, Badrick T. Bayesian approach to guide termination of retrospective retesting after detection of a systematic quality control failure. Clinica Chimica Acta; International Journal of Clinical Chemistry. 437: 52-7. PMID 25034522 DOI: 10.1016/j.cca.2014.07.004 |
0.354 |
|
2014 |
Jiang Y, Park CM, Loh TP. Transition-metal-free synthesis of substituted pyridines via ring expansion of 2-allyl-2H-azirines Organic Letters. 16: 3432-3435. PMID 24949522 DOI: 10.1021/ol501010k |
0.348 |
|
2014 |
Feng C, Loh TP. Rhodium(III)-catalyzed cross-coupling of alkenylboronic acids and N-pivaloyloxylamides. Organic Letters. 16: 3444-7. PMID 24937009 DOI: 10.1021/ol501309e |
0.384 |
|
2014 |
Xu YH, Wu LH, Wang J, Loh TP. Synthesis of multi-substituted vinylsilanes via copper(I)-catalyzed hydrosilylation reactions of allenes and propiolate derivatives with silylboronates. Chemical Communications (Cambridge, England). 50: 7195-7. PMID 24867646 DOI: 10.1039/c4cc01722f |
0.411 |
|
2014 |
Yin P, Wong MY, Tham J, Loh TP. Palladium-catalyzed amination of allylic carbonates with ammonia: access to primary amines Organic Chemistry Frontiers. 1: 1266-1269. DOI: 10.1039/C4Qo00238E |
0.454 |
|
2014 |
Xu YH, Wu LH, Wang J, Loh TP. Synthesis of multi-substituted vinylsilanes via copper(i)-catalyzed hydrosilylation reactions of allenes and propiolate derivatives with silylboronates Chemical Communications. 50: 7195-7197. DOI: 10.1039/c4cc01722f |
0.411 |
|
2014 |
Wang L, Xiao J, Loh TP. Organocatalytic β-functionalization of saturated carbonyl compounds - The state of the art Chemcatchem. 6: 1183-1185. DOI: 10.1002/Cctc.201400010 |
0.441 |
|
2013 |
Zhang YX, Zhang AQ, Tian JS, Loh TP. Diastereoselective oxidative α-amination of aliphatic aldehydes catalyzed by iodine: synthesis of syn-γ-hydroxy-α-amino acetals. Organic & Biomolecular Chemistry. 11: 8387-94. PMID 24186619 DOI: 10.1039/c3ob42043d |
0.306 |
|
2013 |
Zhang X, Wang M, Zhang MX, Xu YH, Loh TP. Synthesis of dienyl ketones via palladium(II)-catalyzed direct cross-coupling reactions between simple alkenes and vinyl ketones: application to the synthesis of vitamin A1 and bornelone. Organic Letters. 15: 5531-3. PMID 24131401 DOI: 10.1021/Ol402692T |
0.324 |
|
2013 |
Shi Z, Loh TP. Organocatalytic synthesis of highly functionalized pyridines at room temperature. Angewandte Chemie (International Ed. in English). 52: 8584-7. PMID 23788467 DOI: 10.1002/Anie.201301519 |
0.327 |
|
2013 |
Zhao B, Loh TP. Asymmetric hetero-Diels-Alder reaction of Danishefsky's dienes with α-carbonyl esters catalyzed by an indium(III)-pybox complex. Organic Letters. 15: 2914-7. PMID 23738771 DOI: 10.1021/ol400841s |
0.374 |
|
2013 |
Zhu MK, Chen YC, Loh TP. Radical-mediated diamination of alkenes with phenylhydrazine and azodicarboxylates: highly diastereoselective synthesis of trans-diamines from cycloalkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 5250-4. PMID 23471689 DOI: 10.1002/chem.201203832 |
0.323 |
|
2013 |
Xu YH, Wang M, Lu P, Loh TP. Palladium-catalyzed alkenyl C-H bond sulfonylation reaction using organosulfonyl chlorides Tetrahedron. 69: 4403-4407. DOI: 10.1016/j.tet.2013.01.071 |
0.313 |
|
2013 |
Lukamto DH, Wang P, Loh T. Catalytic Conversion of Inert Carbohydrates into Platform Chemical 5-Hydroxymethylfurfural Using Arylboronic Acids Asian Journal of Organic Chemistry. 2: 947-951. DOI: 10.1002/Ajoc.201300185 |
0.323 |
|
2012 |
Zhang J, Loh TP. Ruthenium- and rhodium-catalyzed cross-coupling reaction of acrylamides with alkenes: efficient access to (Z,E)-dienamides. Chemical Communications (Cambridge, England). 48: 11232-4. PMID 23069732 DOI: 10.1039/c2cc36137j |
0.362 |
|
2012 |
Li B, Zhao YJ, Lai YC, Loh TP. Asymmetric syntheses of 8-oxabicyclo[3,2,1]octanes: a cationic cascade cyclization. Angewandte Chemie (International Ed. in English). 51: 8041-5. PMID 22865563 DOI: 10.1002/anie.201202699 |
0.346 |
|
2012 |
Shi Z, Yu P, Loh TP, Zhong G. Catalytic asymmetric [4+2] annulation initiated by an aza-Rauhut-Currier reaction: facile entry to highly functionalized tetrahydropyridines. Angewandte Chemie (International Ed. in English). 51: 7825-9. PMID 22833412 DOI: 10.1002/Anie.201203316 |
0.51 |
|
2012 |
Xiao J, Zhao K, Loh TP. The acid free asymmetric intermolecular α-alkylation of aldehydes in fluorinated alcohols. Chemical Communications (Cambridge, England). 48: 3548-50. PMID 22377615 DOI: 10.1039/c2cc30261f |
0.549 |
|
2011 |
Zhu MK, Zhao JF, Loh TP. Palladium-catalyzed C-C bond formation of arylhydrazines with olefins via carbon-nitrogen bond cleavage. Organic Letters. 13: 6308-11. PMID 22054076 DOI: 10.1021/ol202862t |
0.639 |
|
2011 |
Xiao J, Zhao K, Loh TP. Highly enantioselective intermolecular alkylation of aldehydes with alcohols by cooperative catalysis of diarylprolinol silyl ether with Brønsted acid. Chemistry, An Asian Journal. 6: 2890-4. PMID 21954165 DOI: 10.1002/Asia.201100692 |
0.591 |
|
2011 |
Feng C, Loh TP. Rhodium-catalyzed direct ortho C-H olefination of phenol derivatives. Chemical Communications (Cambridge, England). 47: 10458-60. PMID 21850318 DOI: 10.1039/c1cc14108b |
0.369 |
|
2011 |
Li H, Loh TP. A facile synthesis of highly substituted five-membered rings: Mukaiyama-aldol-oxonoium-ene (MAOE) domino reaction. Chemistry, An Asian Journal. 6: 1948-51. PMID 21557483 DOI: 10.1002/asia.201000884 |
0.388 |
|
2011 |
Tian JS, Loh TP. Copper-catalyzed α-amination of aliphatic aldehydes. Chemical Communications (Cambridge, England). 47: 5458-60. PMID 21475752 DOI: 10.1039/c1cc11102g |
0.384 |
|
2011 |
Shen ZL, Goh KK, Wong CH, Yang YS, Lai YC, Cheong HL, Loh TP. Direct synthesis of ester-containing indium homoenolate and its application in palladium-catalyzed cross-coupling with aryl halide. Chemical Communications (Cambridge, England). 47: 4778-80. PMID 21412540 DOI: 10.1039/C0Cc05597B |
0.361 |
|
2011 |
Xiao J, Lu YP, Liu YL, Wong PS, Loh TP. A new class of structurally rigid tricyclic chiral secondary amine organocatalyst: highly enantioselective organocatalytic Michael addition of aldehydes to vinyl sulfones. Organic Letters. 13: 876-9. PMID 21271690 DOI: 10.1021/Ol102933Q |
0.629 |
|
2011 |
Wang SY, Song P, Chin YJ, Loh TP. A general strategy for the introduction of stereogenic centers bearing a methyl group: total synthesis of sex pheromones. Chemistry, An Asian Journal. 6: 385-8. PMID 21254416 DOI: 10.1002/Asia.201000663 |
0.327 |
|
2011 |
Wang P, Yeo XL, Loh TP. Copper-catalyzed highly regioselective silylcupration of terminal alkynes to form α-vinylsilanes. Journal of the American Chemical Society. 133: 1254-6. PMID 21208005 DOI: 10.1021/ja109464u |
0.323 |
|
2011 |
Shen ZL, Lai YC, Wong CH, Goh KK, Yang YS, Cheong HL, Loh TP. Palladium-catalyzed cross-coupling of indium homoenolate with aryl halide with wide functional group compatibility. Organic Letters. 13: 422-5. PMID 21182334 DOI: 10.1021/Ol102755Q |
0.366 |
|
2011 |
Shen ZL, Goh KK, Yang YS, Lai YC, Wong CH, Cheong HL, Loh TP. Direct synthesis of water-tolerant alkyl indium reagents and their application in palladium-catalyzed couplings with aryl halides. Angewandte Chemie (International Ed. in English). 50: 511-4. PMID 21132827 DOI: 10.1002/Anie.201005798 |
0.347 |
|
2011 |
Sampath M, Lee PB, Loh T. Phosphine-catalyzed one-pot isomerization of 3-alkynoates and [2 + 3]-cycloaddition with imines: formal synthesis of Securinegaalkaloid (±)-allosecurinine Chemical Science. 2: 1988-1991. DOI: 10.1039/C1Sc00311A |
0.451 |
|
2011 |
Xu Y, Chok YK, Loh T. Synthesis and characterization of a cyclic vinylpalladium( ii ) complex: vinylpalladium species as the possible intermediate in the catalytic direct olefination reaction of enamide Chemical Science. 2: 1822-1825. DOI: 10.1039/C1Sc00262G |
0.475 |
|
2011 |
Zhao JF, Tan BH, Loh TP. In(III)-pybox complex catalyzed enantioselective Mukaiyama aldol reactions between polymeric or hydrated glyoxylates and enolsilanes derived from aryl ketones Chemical Science. 2: 349-352. DOI: 10.1039/C0Sc00454E |
0.528 |
|
2010 |
Feng C, Loh TP. Palladium-catalyzed bisolefination of C-C triple bonds: a facile method for the synthesis of naphthalene derivatives. Journal of the American Chemical Society. 132: 17710-2. PMID 21114296 DOI: 10.1021/Ja108998D |
0.458 |
|
2010 |
Wang SY, Loh TP. Highly enantioselective Cu(I)-Tol-BINAP-catalyzed asymmetric conjugate addition of Grignard reagents to α,β-unsaturated esters. Chemical Communications (Cambridge, England). 46: 8694-703. PMID 21038042 DOI: 10.1039/c0cc03211e |
0.348 |
|
2010 |
Wang SY, Song P, Chan LY, Loh TP. Total synthesis of Phytophthora mating hormone α1. Organic Letters. 12: 5166-9. PMID 20973505 DOI: 10.1021/Ol102177J |
0.378 |
|
2010 |
Shen ZL, Goh KK, Cheong HL, Wong CH, Lai YC, Yang YS, Loh TP. Synthesis of water-tolerant indium homoenolate in aqueous media and its application in the synthesis of 1,4-dicarbonyl compounds via palladium-catalyzed coupling with acid chloride. Journal of the American Chemical Society. 132: 15852-5. PMID 20964387 DOI: 10.1021/Ja106925F |
0.403 |
|
2010 |
Tian JS, Loh TP. Copper-catalyzed rearrangement of tertiary amines through oxidation of aliphatic C-H bonds in air or oxygen: direct synthesis of α-amino acetals. Angewandte Chemie (International Ed. in English). 49: 8417-20. PMID 20878822 DOI: 10.1002/Anie.201003646 |
0.392 |
|
2010 |
Zhao YJ, Li B, Tan LJ, Shen ZL, Loh TP. Enantioselective cationic polyene cyclization vs enantioselective intramolecular carbonyl-ene reaction. Journal of the American Chemical Society. 132: 10242-4. PMID 20614887 DOI: 10.1021/ja104119j |
0.426 |
|
2010 |
Li H, Loh TP. A facile method for the synthesis of highly substituted six-membered rings: Mukaiyama-Aldol-Prins cascade reaction. Organic Letters. 12: 2679-81. PMID 20481623 DOI: 10.1021/ol100937r |
0.385 |
|
2010 |
Zhu MK, Zhao JF, Loh TP. Palladium-catalyzed oxime assisted intramolecular dioxygenation of alkenes with 1 atm of air as the sole oxidant. Journal of the American Chemical Society. 132: 6284-5. PMID 20394368 DOI: 10.1021/Ja100716X |
0.668 |
|
2010 |
Xiao J, Xu FX, Lu YP, Loh TP. Chemzymes: a new class of structurally rigid tricyclic amphibian organocatalyst inspired by natural product. Organic Letters. 12: 1220-3. PMID 20158252 DOI: 10.1021/ol9029758 |
0.532 |
|
2010 |
Loh T, Xiao J, Liu Y. The Organocatalytic Enantioselective Michael Addition of Aldehydes to Vinyl Sulfones in Water Synlett. 2010: 2029-2032. DOI: 10.1055/S-0030-1258483 |
0.607 |
|
2010 |
Luo H, Hu X, Loh T. Highly stereocontrolled synthesis of fluorinated 2,6-trans dihydropyrans via Prins cyclization Tetrahedron Letters. 51: 1041-1043. DOI: 10.1016/J.Tetlet.2009.12.068 |
0.467 |
|
2010 |
Wang S, Song P, Loh T. Excess Phosphine Ligand Plays a Critical Role in the Asymmetric Copper(I) Iodide‐Catalyzed Conjugate Addition of Grignard Reagents to α,β‐Unsaturated Esters Advanced Synthesis & Catalysis. 352: 3185-3189. DOI: 10.1002/Adsc.201000631 |
0.402 |
|
2009 |
Zhao JF, Tjan TB, Tan BH, Loh TP. Highly enantioselective ketone-ene reactions of trifluoropyruvate: significant counterion effect of the In(III)-pybox complex. Organic Letters. 11: 5714-6. PMID 19911807 DOI: 10.1021/ol902507x |
0.738 |
|
2009 |
Zhao JF, Loh TP. Acid-catalyzed intramolecular [2+2] cycloaddition of ene-allenones: facile access to bicyclo[n.2.0] frameworks. Angewandte Chemie (International Ed. in English). 48: 7232-5. PMID 19718730 DOI: 10.1002/anie.200902471 |
0.662 |
|
2009 |
Chin YJ, Wang SY, Loh TP. Synthesis of iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction. Organic Letters. 11: 3674-6. PMID 19627100 DOI: 10.1021/Ol901480S |
0.379 |
|
2009 |
Zhao YJ, Tan LJ, Li B, Li SM, Loh TP. Bio-inspired polyene cyclization: aziridinyl polyene cyclization catalyzed by InBr(3). Chemical Communications (Cambridge, England). 3738-40. PMID 19557266 DOI: 10.1039/B903696B |
0.48 |
|
2009 |
Zhou H, Xu YH, Chung WJ, Loh TP. Palladium-catalyzed direct arylation of cyclic enamides with aryl silanes by sp(2) C-H activation. Angewandte Chemie (International Ed. in English). 48: 5355-7. PMID 19533704 DOI: 10.1002/Anie.200901884 |
0.317 |
|
2009 |
Xiao J, Loh TP. Design, synthesis and optical resolution of new bifunctional ligand: 1,1'-dimethyl-octahydro-8,8'-biquinoline-7,7'-diol. Organic Letters. 11: 2876-9. PMID 19476338 DOI: 10.1021/Ol900790Z |
0.534 |
|
2009 |
Hu XH, Liu F, Loh TP. Stereoelectronic versus steric tuning in the prins cyclization reaction: synthesis of 2,6-trans pyranyl motifs. Organic Letters. 11: 1741-3. PMID 19301864 DOI: 10.1021/ol900196w |
0.407 |
|
2009 |
Sampath M, Loh TP. Silicon as a directing group in the phosphine-catalyzed [2+3]-cycloaddition of aryl allenones with electron-deficient olefins. Chemical Communications (Cambridge, England). 1568-70. PMID 19277392 DOI: 10.1039/b819959k |
0.336 |
|
2009 |
Yang YS, Shen ZL, Loh TP. Indium (zinc)-copper-mediated Barbier-type alkylation reaction of nitrones in water: synthesis of amines and hydroxylamines. Organic Letters. 11: 1209-12. PMID 19215084 DOI: 10.1021/ol8027362 |
0.336 |
|
2009 |
Xu YH, Lu J, Loh TP. Direct cross-coupling reaction of simple alkenes with acrylates catalyzed by palladium catalyst. Journal of the American Chemical Society. 131: 1372-3. PMID 19132899 DOI: 10.1021/Ja8084548 |
0.472 |
|
2009 |
Wang S, Chin Y, Loh T. Synthesis of C13-C23Fragment of Iriomoteolide-1a Synthesis. 2009: 3557-3564. DOI: 10.1055/S-0029-1218152 |
0.453 |
|
2009 |
Fu F, Loh TP. An asymmetric synthesis of the polyol fragment of the polyene macrolide antibiotic RK-397 Tetrahedron Letters. 50: 3530-3533. DOI: 10.1016/J.Tetlet.2009.03.019 |
0.452 |
|
2009 |
Luo H, Loh T. Synthesis of aryl allylic fluorides by direct electrophilic fluorination of alkenes Tetrahedron Letters. 50: 1554-1556. DOI: 10.1016/J.Tetlet.2009.01.052 |
0.491 |
|
2008 |
Zhao JF, Tsui HY, Wu PJ, Lu J, Loh TP. Highly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex. Journal of the American Chemical Society. 130: 16492-3. PMID 19554724 DOI: 10.1021/Ja807501A |
0.76 |
|
2008 |
Zhao YJ, Loh TP. Bioinspired polyene cyclization promoted by intermolecular chiral acetal-SnCl4 or chiral N-acetal-TiCl4: investigation of the mechanism and identification of the key intermediates. Journal of the American Chemical Society. 130: 10024-9. PMID 18605726 DOI: 10.1021/Ja802896N |
0.499 |
|
2008 |
Cheng HS, Seow AH, Loh TP. Homoallyllic nitrone isomerization: convenient enantioselective synthesis of homoallylic nitrones and homoallylic hydroxylamines. Organic Letters. 10: 2805-7. PMID 18537248 DOI: 10.1021/Ol800925V |
0.527 |
|
2008 |
Li H, Loh TP. Control of up to five stereocenters in a cascade reaction: synthesis of highly functionalized five-membered rings. Journal of the American Chemical Society. 130: 7194-5. PMID 18489092 DOI: 10.1021/ja801488z |
0.393 |
|
2008 |
Zhao YJ, Loh TP. Asymmetric total synthesis of antiochic acid. Organic Letters. 10: 2143-5. PMID 18439020 DOI: 10.1021/Ol800499P |
0.438 |
|
2008 |
Shen ZL, Yeo YL, Loh TP. Indium-copper and indium-silver mediated barbier-grignard-type alkylation reaction of aldehydes using unactivated alkyl halides in water. The Journal of Organic Chemistry. 73: 3922-4. PMID 18396908 DOI: 10.1021/jo8000589 |
0.328 |
|
2008 |
Zhao JF, Zhao YJ, Loh TP. Indium tribromide-promoted arene-terminated epoxy olefin cyclization. Chemical Communications (Cambridge, England). 1353-5. PMID 18389131 DOI: 10.1039/b718337b |
0.681 |
|
2008 |
Zhao YJ, Loh TP. Bio-inspired polyene cyclization: synthesis of tetracyclic terpenoids promoted by steroidal acetal-SnCl4. Chemical Communications (Cambridge, England). 1434-6. PMID 18338047 DOI: 10.1039/b714474a |
0.337 |
|
2008 |
Lum TK, Wang SY, Loh TP. A highly catalytic asymmetric conjugate addition: synthesis of the C14-C20 fragment of antibiotic TMC-151A, siphonarienal and siphonarienone. Organic Letters. 10: 761-4. PMID 18229932 DOI: 10.1021/Ol702715Q |
0.416 |
|
2008 |
Shen ZL, Cheong HL, Loh TP. Indium-silver- and zinc-silver-mediated barbier-grignard-type alkylation reactions of imines by using unactivated alkyl halides in aqueous media. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 1875-80. PMID 18058963 DOI: 10.1002/chem.200701468 |
0.411 |
|
2008 |
Zhao YJ, Loh TP. Practical synthesis of 1,5-dimethyl substituted conjugated polyenes from geranyl acetate Tetrahedron. 64: 4972-4978. DOI: 10.1016/J.Tet.2008.03.094 |
0.426 |
|
2008 |
Lu J, Liu F, Zhou W, Loh T. ChemInform Abstract: Enantioselective Direct Vinylogous Michael Addition Reaction Catalyzed by Organic Molecules. Cheminform. 39. DOI: 10.1002/CHIN.200852102 |
0.331 |
|
2008 |
Lu J, Zhou W, Liu F, Loh T. ChemInform Abstract: Organocatalytic and Enantioselective Direct Vinylogous Michael Addition to Maleimides. Cheminform. 39. DOI: 10.1002/CHIN.200851095 |
0.318 |
|
2007 |
Shen ZL, Loh TP. Indium-copper-mediated barbier-grignard-type alkylation reaction of imines in aqueous media. Organic Letters. 9: 5413-6. PMID 18052071 DOI: 10.1021/Ol702263B |
0.512 |
|
2007 |
Chan KP, Ling YH, Loh TP. Formal synthesis of (+)-SCH 351448: the Prins cyclization approach. Chemical Communications (Cambridge, England). 939-41. PMID 17311127 DOI: 10.1039/B616558C |
0.44 |
|
2007 |
Zhao YJ, Chng SS, Loh TP. Lewis Acid-promoted intermolecular acetal-initiated cationic polyene cyclizations. Journal of the American Chemical Society. 129: 492-3. PMID 17227003 DOI: 10.1021/Ja067660+ |
0.441 |
|
2007 |
Wang SY, Ji SJ, Loh TP. Cu(I) Tol-BINAP-catalyzed enantioselective Michael reactions of Grignard reagents and unsaturated esters. Journal of the American Chemical Society. 129: 276-7. PMID 17212398 DOI: 10.1021/Ja0666046 |
0.49 |
|
2007 |
Fu F, Teo YC, Loh TP. Catalytic enantioselective Diels-Alder reaction in ionic liquid via a recyclable chiral In(III) complex. Organic Letters. 8: 5999-6001. PMID 17165914 DOI: 10.1021/ol062481i |
0.343 |
|
2007 |
Lee WW, Gan L, Loh T. Microwave-assisted synthesis of photochromic fulgimides Journal of Photochemistry and Photobiology a-Chemistry. 185: 106-109. DOI: 10.1016/J.Jphotochem.2006.05.018 |
0.355 |
|
2006 |
Lee K, Loh T. Total synthesis of antillatoxin. Chemical Communications. 4209-4211. PMID 17031434 DOI: 10.1039/B608193M |
0.379 |
|
2006 |
Teo YC, Goh JD, Loh TP. Catalytic enantioselective allylation of ketones via a chiral indium(III) complex. Organic Letters. 7: 2743-5. PMID 15957936 DOI: 10.1021/ol051018n |
0.38 |
|
2006 |
Teo YC, Loh TP. Catalytic enantioselective Diels-Alder reaction via a chiral indium(III) complex. Organic Letters. 7: 2539-41. PMID 15957885 DOI: 10.1021/OL050518D |
0.43 |
|
2006 |
Lu J, Ji SJ, Teo YC, Loh TP. Highly enantioselective allylation of aldehydes catalyzed by indium(III)-PYBOX complex. Organic Letters. 7: 159-61. PMID 15625002 DOI: 10.1021/OL047711C |
0.341 |
|
2006 |
Lee CA, Loh T. Suppression of epimerization due to selectivity leakage: an application towards the total synthesis of (−)-centrolobine Tetrahedron Letters. 47: 1641-1644. DOI: 10.1016/J.Tetlet.2005.12.108 |
0.404 |
|
2006 |
Lee CA, Loh T. A highly enantioselective one-pot synthesis of homoallylic alcohols via tandem asymmetric allyl transfer/olefin cross metathesis Tetrahedron Letters. 47: 809-812. DOI: 10.1016/J.Tetlet.2005.11.078 |
0.477 |
|
2006 |
Lu J, Ji S, Teo Y, Loh T. Asymmetric Allyltributylstannane Addition to Ketones Catalyzed by Chiral PYBOX—In(III) Complex Immobilized in Ionic Liquid. Cheminform. 37. DOI: 10.1016/J.Tetlet.2005.08.090 |
0.439 |
|
2006 |
Lu J, Hong M, Ji S, Teo Y, Loh T. Enantioselective Allylation of Ketones Catalyzed by Chiral In(III)-PYBOX Complexes. Cheminform. 37. DOI: 10.1002/CHIN.200603032 |
0.333 |
|
2005 |
Chan KP, Loh TP. Prins cyclizations in silyl additives with suppression of epimerization: Versatile tool in the synthesis of the tetrahydropyran backbone of natural products Organic Letters. 7: 4491-4494. PMID 16178566 DOI: 10.1021/ol051951q |
0.343 |
|
2005 |
Lu J, Hong ML, Ji SJ, Teo YC, Loh TP. Enantioselective allylation of ketones catalyzed by chiral In(III)-PYBOX complexes. Chemical Communications (Cambridge, England). 4217-8. PMID 16100608 DOI: 10.1039/b507768k |
0.356 |
|
2005 |
Lee CK, Loh T. Gram-scale synthesis of (-)-epibatidine. Organic Letters. 7: 2965-2967. PMID 15987181 DOI: 10.1021/Ol050891L |
0.367 |
|
2005 |
Lu J, Ji SJ, Loh TP. Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids. Chemical Communications (Cambridge, England). 2345-7. PMID 15877123 DOI: 10.1039/B500086F |
0.428 |
|
2005 |
Teo Y, Tan K, Loh T. Catalytic asymmetric allylation of aldehydes via a chiral indium(III) complex Chemical Communications. 1318-1320. PMID 15742064 DOI: 10.1039/B412736F |
0.472 |
|
2005 |
Lu J, Hong ML, Ji SJ, Loh TP. Enantioselective synthesis of homoallylic alcohols via a chiral In(III)-PYBOX complex Chemical Communications. 1010-1012. PMID 15719099 DOI: 10.1039/B415550E |
0.418 |
|
2005 |
Cheng H, Loh T. General and practical approach to the syntheses of linear homoallylic alcohols Pure and Applied Chemistry. 77: 1199-1206. DOI: 10.1351/Pac200577071199 |
0.408 |
|
2005 |
Lee WW, Gan L, Loh T. Synthesis and Photochromic Properties of Cycloalkylidene Fulgides Synlett. 2005: 2473-2477. DOI: 10.1055/S-2005-917082 |
0.347 |
|
2005 |
Gu D, Ji S, Jiang Z, Zhou M, Loh T. An Efficient Synthesis of Bis(indolyl)methanes Catalyzed by Recycled Acidic Ionic Liquid Synlett. 2005: 959-962. DOI: 10.1055/S-2005-865194 |
0.47 |
|
2005 |
Lu J, Hong ML, Ji SJ, Teo YC, Loh TP. Enantioselective allylation of ketones catalyzed by chiral In(III)-PYBOX complexes Chemical Communications. 4217-4218. DOI: 10.1039/B507768K |
0.463 |
|
2005 |
Teo Y, Goh E, Loh T. Catalytic enantioselective allylation of aldehydes via a moisture-tolerant chiral BINOL–In(III) complex Tetrahedron Letters. 46: 6209-6211. DOI: 10.1016/J.Tetlet.2005.07.064 |
0.475 |
|
2005 |
Teo Y, Goh E, Loh T. Catalytic enantioselective allylation of aldehydes via a chiral indium(III) complex in ionic liquids Tetrahedron Letters. 46: 4573-4575. DOI: 10.1016/J.Tetlet.2005.05.014 |
0.489 |
|
2005 |
Lu J, Ji S, Teo Y, Loh T. Highly Enantioselective Allylation of Aldehydes Catalyzed by Indium(III)?PYBOX Complex. Cheminform. 36. DOI: 10.1002/CHIN.200520031 |
0.317 |
|
2004 |
Chng SS, Hoang TG, Wayne Lee WW, Tham MP, Ling HY, Loh TP. Synthetic studies towards anti-SARS agents: application of an indium-mediated allylation of α-aminoaldehydes as the key step towards an intermediate. Tetrahedron Letters. 45: 9501-9504. PMID 32287437 DOI: 10.1016/J.Tetlet.2004.10.146 |
0.405 |
|
2004 |
Lee K, Lin M, Loh T. Silicon-assisted propargylic transfer to aldehydes. Chemical Communications. 2456-2457. PMID 15514813 DOI: 10.1039/B411653D |
0.332 |
|
2004 |
Ken Lee CL, Ling HY, Loh TP. Asymmetric synthesis of C-aliphatic homoallylic amines and biologically important cyclohexenylamine analogues. The Journal of Organic Chemistry. 69: 7787-9. PMID 15498019 DOI: 10.1021/jo048903o |
0.372 |
|
2004 |
Chen S, Hu Q, Loh T. Highly efficient chemical kinetic resolution of bishomoallylic alcohols: synthesis of (R)-sulcatol. Organic Letters. 6: 3365-3367. PMID 15355053 DOI: 10.1021/Ol048608Q |
0.393 |
|
2004 |
Lee CK, Lee CA, Tan K, Loh T. An unusual approach to the synthesis of enantiomerically cis linear homoallylic alcohols based on the steric interaction mechanism of camphor scaffold. Organic Letters. 6: 1281-1283. PMID 15070317 DOI: 10.1021/Ol049633Z |
0.39 |
|
2004 |
Ji S, Jiang Z, Lu J, Loh T. Facile Ionic Liquids-Promoted One-Pot Synthesis of Polyhydroquinoline Derivatives under Solvent-Free Conditions. Cheminform. 35. DOI: 10.1055/S-2004-820035 |
0.44 |
|
2004 |
Juan S, Hua Z, Qi S, Ji S, Loh T. Indium trichloride-catalyzed indium-mediated allylation of dihydropyrans and dihydrofurans in water Synlett. 2004: 829-830. DOI: 10.1055/S-2004-820030 |
0.493 |
|
2004 |
Lu J, Ji S, Qian R, Chen J, Liu Y, Loh T. InCl3-Promoted Allylation of Aldehydes in Ionic Liquid: Scope and Enantioselectivity Studies. Cheminform. 35. DOI: 10.1055/S-2004-815433 |
0.493 |
|
2004 |
Chan KP, Loh TP. Lewis acid-catalyzed one-pot crossed Prins cyclizations using allylchlorosilane as allylating agent Tetrahedron Letters. 45: 8387-8390. DOI: 10.1016/J.Tetlet.2004.09.049 |
0.447 |
|
2004 |
Lee CA, Loh T. A highly enantioselective allyl-transfer through suppression of epimerization☆ Tetrahedron Letters. 45: 5819-5822. DOI: 10.1016/J.Tetlet.2004.06.014 |
0.477 |
|
2004 |
Chen S, Ji S, Loh T. Mukaiyama aldol reaction using ketene silyl acetals with carbonyl compounds in ionic liquids Tetrahedron Letters. 45: 375-377. DOI: 10.1016/J.Tetlet.2003.10.155 |
0.46 |
|
2004 |
Ji S, Wang S, Zhang Y, Loh T. Facile synthesis of bis(indolyl)methanes using catalytic amount of iodine at room temperature under solvent-free conditions Tetrahedron. 60: 2051-2055. DOI: 10.1016/J.Tet.2003.12.060 |
0.497 |
|
2004 |
Ji S, Zhou M, Gu D, Jiang Z, Loh T. Efficient FeIII‐Catalyzed Synthesis of Bis(indolyl)methanes in Ionic Liquids European Journal of Organic Chemistry. 2004: 1584-1587. DOI: 10.1002/Ejoc.200300719 |
0.421 |
|
2003 |
Lin M, Loh T. Indium-mediated reaction of trialkylsilyl propargyl bromide with aldehydes: Highly regioselective synthesis of allenic and homopropargylic alcohols Journal of the American Chemical Society. 125: 13042-13043. PMID 14570474 DOI: 10.1021/Ja037410I |
0.413 |
|
2003 |
Cheng H, Loh T. A Novel and General α-Regioselective and Highly Enantioselective Prenylation of Aldehydes Journal of the American Chemical Society. 125: 4990-4991. PMID 12708844 DOI: 10.1021/Ja029700P |
0.493 |
|
2003 |
Tan KT, Chng SS, Cheng HS, Loh TP. Development of a highly alpha-regioselective metal-mediated allylation reaction in aqueous media: new mechanistic proposal for the origin of alpha-homoallylic alcohols. Journal of the American Chemical Society. 125: 2958-63. PMID 12617663 DOI: 10.1021/Ja029276S |
0.312 |
|
2003 |
Huang J, Xu K, Loh T. Indium-mediated allylation reaction in aqueous media: Synthetic studies towards the total synthesis of dysiherbaine Synthesis. 2003: 755-764. DOI: 10.1055/S-2003-38058 |
0.508 |
|
2003 |
Chng S, Xu J, Loh T. A divergent approach to apoptolidin and FD-891: asymmetric preparation of a common intermediate Tetrahedron Letters. 44: 4997-5000. DOI: 10.1016/S0040-4039(03)01173-0 |
0.436 |
|
2003 |
Loh T, Lin M, Tan K. Indium-mediated propargylation of aldehydes: regioselectivity and enantioselectivity studies Tetrahedron Letters. 44: 507-509. DOI: 10.1016/S0040-4039(02)02613-8 |
0.486 |
|
2002 |
Loh T, Chen S. InCl3-Catalyzed Three-Component Asymmetric Mannich-Type Reaction in Methanol Organic Letters. 4: 3647-3650. PMID 12375909 DOI: 10.1021/Ol0265968 |
0.478 |
|
2002 |
Loh T, Lee CK, Tan K. The first example of enantioselective allyl transfer from a linear homoallylic alcohol to an aldehyde. Organic Letters. 4: 2985-2987. PMID 12182605 DOI: 10.1021/Ol0263999 |
0.377 |
|
2002 |
Loh T, Song H, Zhou Y. Nickel-Catalyzed Homoallylation Reaction of Aldehydes with 1,3-Dienes: Stereochemical and Mechanistic Studies Organic Letters. 4: 2715-2717. PMID 12153217 DOI: 10.1021/Ol026216I |
0.5 |
|
2002 |
Loh TP, Hu QY, Ma LT. Stereocontrolled synthesis of linear 22R-homoallylic sterols via a triflic acid-catalyzed 2-oxonia Cope rearrangement. Organic Letters. 4: 2389-91. PMID 12098254 DOI: 10.1021/ol026136e |
0.371 |
|
2002 |
Loh T, Song H. Studies Towards Total Synthesis of Antillatoxin: Indium-mediated Allylation Reaction of Carbonyl Compounds with Secondary Allylic Bromide in Aqueous Media Synlett. 2002: 2119-2121. DOI: 10.1055/S-2002-35606 |
0.524 |
|
2002 |
Loh T, Feng L, Yang J. Indium(III) complex-catalyzed tandem carbonyl-ene reaction: An efficient construction of tetrahydropyran rings Synthesis. 2002: 937-940. DOI: 10.1055/S-2002-28501 |
0.434 |
|
2001 |
Loh TP, Tan KT, Hu QY. The First In(OTf) -Catalyzed Conversion of Kinetically Formed Homoallylic Alcohols into the Thermodynamically Preferred Regioisomers: Application to the Synthesis of 22α-Sterols. Angewandte Chemie (International Ed. in English). 40: 2921-2922. PMID 29711997 DOI: 10.1002/1521-3773(20010803)40:15<2921::AID-ANIE2921>3.0.CO;2-V |
0.339 |
|
2001 |
Loh TP, Hu QY, Tan KT, Cheng HS. Diverse cyclization catalyzed by In(OTf)3 for the convergent assembly of substituted tetrahydrofurans and tetrahydropyrans. Organic Letters. 3: 2669-72. PMID 11506605 DOI: 10.1021/Ol016228O |
0.486 |
|
2001 |
Loh T, Tan K, Hu Q. A new mechanistic proposal for the origin of α-homoallylic alcohols in indium-mediated allylation reactions in water Tetrahedron Letters. 42: 8705-8708. DOI: 10.1016/S0040-4039(01)01884-6 |
0.43 |
|
2001 |
Loh T, Chok Y, Yin Z. Synthetic studies toward kaitocephalin Tetrahedron Letters. 42: 7893-7897. DOI: 10.1016/S0040-4039(01)01631-8 |
0.487 |
|
2001 |
Loh T, Feng L. Progress towards the total synthesis of tedanolide: an efficient assembly of the C1–C11 subunit Tetrahedron Letters. 42: 6001-6005. DOI: 10.1016/S0040-4039(01)01169-8 |
0.37 |
|
2001 |
Loh T, Lye P. A concise synthesis of (±)-methylenolactocin and the formal synthesis of (±)-phaseolinic acid Tetrahedron Letters. 42: 3511-3514. DOI: 10.1016/S0040-4039(01)00492-0 |
0.348 |
|
2001 |
Loh T, Feng L. Synthetic studies towards the total synthesis of tedanolide: formation of the C(13)–C(23) fragment Tetrahedron Letters. 42: 3223-3226. DOI: 10.1016/S0040-4039(01)00401-4 |
0.372 |
|
2001 |
Loh TP, Feng LC, Wei LL. InCl3-Catalyzed direct aldol reactions of glyoxylic acid monohydrate and glyoxylates with various ketones: Scope and limitations Tetrahedron. 57: 4231-4236. DOI: 10.1016/S0040-4020(01)00309-X |
0.485 |
|
2000 |
Loh TP, Huang JM, Goh SH, Vittal JJ. Aldol reaction under solvent-free conditions: highly stereoselective synthesis of 1,3-amino alcohols Organic Letters. 2: 1291-4. PMID 10810730 DOI: 10.1021/Ol000042S |
0.486 |
|
2000 |
Loh T, Hu Q, Vittal JJ. Indium-Mediated Allylation: Application to the Synthesis of 22-Hydroxy Steroids Synlett. 2000: 523-525. DOI: 10.1055/S-2000-6579 |
0.407 |
|
2000 |
Loh T, Xu J, Hu Q, Vittal JJ. A highly chemoselective and diastereoselective trifluoromethane sulfonic acid catalyzed addition of allyltributylstannanes to a steroidal aldehyde in aqueous media Tetrahedron: Asymmetry. 11: 1565-1569. DOI: 10.1016/S0957-4166(00)00088-4 |
0.455 |
|
2000 |
Loh T, Lye P, Wang R, Sim K. A highly regioselective indium-mediated allylation of pyridine derivatives: synthesis of (±)-dihydropinidine from pyridine Tetrahedron Letters. 41: 7779-7783. DOI: 10.1016/S0040-4039(00)01332-0 |
0.385 |
|
2000 |
Loh T, Huang J, Xu K, Goh S, Vittal JJ. A remote substituent as a control element in indium-mediated allylation reactions in aqueous media: highly diastereoselective synthesis of 1,3-amino alcohols Tetrahedron Letters. 41: 6511-6515. DOI: 10.1016/S0040-4039(00)01040-6 |
0.439 |
|
2000 |
Loh T, Zhou J. A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium Tetrahedron Letters. 41: 5261-5264. DOI: 10.1016/S0040-4039(00)00801-7 |
0.711 |
|
2000 |
Loh T, Feng L, Wei L. Water-Accelerated Aldol Reaction of Ketene Silyl Acetals with Carbonyl Compounds Tetrahedron. 56: 7309-7312. DOI: 10.1016/S0040-4020(00)00630-X |
0.48 |
|
1999 |
Loh T, Wei L, Feng L. Direct Aldol Reactions of Glycoxylic Acid Monohydrate with Ketones Synlett. 1999: 1059-1060. DOI: 10.1055/S-1999-2786 |
0.449 |
|
1999 |
Loh T, Zhou J, Yin Z. A Highly Enantioselective Indium-Mediated Allylation Reaction of Aldehydes Organic Letters. 1: 1855-1857. DOI: 10.1021/Ol990316F |
0.502 |
|
1999 |
Loh T, Zhou J, Li X. An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane Tetrahedron Letters. 40: 9333-9336. DOI: 10.1016/S0040-4039(99)01976-0 |
0.72 |
|
1999 |
Loh T, Koh KS, Sim K, Leong W. Competitive fine-tuning of heteroaromatic imines as dienophiles or dienes in the Lewis acid-mediated Diels-Alder reaction with cyclopentadiene Tetrahedron Letters. 40: 8447-8451. DOI: 10.1016/S0040-4039(99)01770-0 |
0.472 |
|
1999 |
Loh T, Zhou J. An enantioselective allylation reaction of aldehydes in an aqueous medium Tetrahedron Letters. 40: 9115-9118. DOI: 10.1016/S0040-4039(99)01743-8 |
0.707 |
|
1999 |
Loh T, Zhou J, Li X, Sim K. A novel reductive aminocyclization for the syntheses of chiral pyrrolidines: stereoselective syntheses of (S)-nornicotine and 2-(2′-pyrrolidyl)-pyridines Tetrahedron Letters. 40: 7847-7850. DOI: 10.1016/S0040-4039(99)01606-8 |
0.678 |
|
1999 |
Loh T, Cao G, Yin Z. A new method for the synthesis of β,γ-unsaturated amides from allylic carbonate catalyzed by palladium in the presence of carbon monoxide and amine: Studies towards the total synthesis of antillatoxin Tetrahedron Letters. 40: 2649-2652. DOI: 10.1016/S0040-4039(99)00264-6 |
0.41 |
|
1999 |
Loh T, Xu J. Trifluoromethane sulphonic acid: a Brönsted acid catalyst for the addition of allyltributylstannanes to carbonyl compounds in water Tetrahedron Letters. 40: 2431-2434. DOI: 10.1016/S0040-4039(99)00122-7 |
0.37 |
|
1999 |
Loh T, Li X. Clay montmorillonite K10 catalyzed aldol-type reaction of aldehydes with silyl enol ethers in water Tetrahedron. 55: 10789-10802. DOI: 10.1016/S0040-4020(99)00594-3 |
0.367 |
|
1999 |
Loh T, Li X. A simple and practical synthesis of α-trifluoromethylated alcohols in water Tetrahedron. 55: 5611-5622. DOI: 10.1016/S0040-4020(99)00227-6 |
0.446 |
|
1999 |
Loh T, Li X. Tin- and Indium-Mediated Allylation Reactions in Water: Highly Stereoselective Synthesis of β-Trifluoromethylated Homoallylic Alcohols European Journal of Organic Chemistry. 1999: 1893-1899. DOI: 10.1002/(Sici)1099-0690(199908)1999:8<1893::Aid-Ejoc1893>3.0.Co;2-3 |
0.464 |
|
1998 |
Loh T, Wei L. Indium Trichloride-Catalyzed Conjugate Addition of Amines to α,β-Ethylenic Compounds in Water Synlett. 1998: 975-976. DOI: 10.1055/S-1998-1845 |
0.353 |
|
1998 |
Loh T, Xu K, Ho DS, Sim K. Indium Trifluoride - A Lewis Acid Catalyst For The Addition Of TMSCN To Aldehydes In Water Synlett. 1998: 369-370. DOI: 10.1055/S-1998-1676 |
0.339 |
|
1998 |
Loh T, Chua G, Vittal JJ, Wong M. Highly stereoselective indium trichloride-catalysed asymmetric aldol reaction of formaldehyde and a glucose-derived silyl enol ether in water Chemical Communications. 861-871. DOI: 10.1039/A800486B |
0.419 |
|
1998 |
Loh T, Cao G, Pei J. Studies towards total synthesis of antillatoxin: Synthesis of C1C11 fragment Tetrahedron Letters. 39: 1457-1460. DOI: 10.1016/S0040-4039(97)10827-9 |
0.604 |
|
1998 |
Loh T, Cao G, Pei J. Studies towards total synthesis of antillatoxin: Investigation of the indium-mediated allylation reactions of carbonyl compounds with β-bromocrotylbromide in water Tetrahedron Letters. 39: 1453-1456. DOI: 10.1016/S0040-4039(97)10826-7 |
0.565 |
|
1998 |
Loh TP, Wei LL. Novel one-pot Mannich-type reaction in water: Indium trichloride-catalyzed condensation of aldehydes, amines and silyl enol ethers for the synthesis of β-amino ketones and esters Tetrahedron Letters. 39: 323-326. DOI: 10.1016/S0040-4039(97)10478-6 |
0.517 |
|
1998 |
Loh TP, Wei LL. Indium-trichloride catalyzed Michael reaction of silyl enol ethers with α,β-unsaturated carbonyl compounds under neat condition Tetrahedron. 54: 7615-7624. DOI: 10.1016/S0040-4020(98)00394-9 |
0.468 |
|
1997 |
Loh T, Ho DS, Chua G, Sim K. A New Stereoselective Route to Chiral Tertiary Alcohols in Water Synlett. 1997: 563-564. DOI: 10.1055/S-1997-3230 |
0.342 |
|
1997 |
Srikanth N, Tan CH, Ng SC, Loh TP, Koh LL, Sim KY. Synthesis of Heterocyclic Analogues of Tamoxifen as Potential Antiestrogens Journal of Chemical Research - Part S. 274-275. DOI: 10.1039/A701410D |
0.648 |
|
1997 |
Loh T, Pei J, Koh KS, Cao G, Li X. Indium-trichloride catalyzed mukaiyama-aldol reaction in water: Solubility, aggregation and internal pressure effect Tetrahedron Letters. 38: 3465-3468. DOI: 10.1016/S0040-4039(97)00595-9 |
0.506 |
|
1997 |
Loh T, Li X. A novel method for stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water Tetrahedron Letters. 38: 869-872. DOI: 10.1016/S0040-4039(96)02434-3 |
0.434 |
|
1997 |
Loh T, Li X. A Highly Stereoselective Synthesis ofβ-Trifluoromethylated Homoallylic Alchols in Water Angewandte Chemie International Edition in English. 36: 980-982. DOI: 10.1002/Anie.199709801 |
0.372 |
|
1997 |
Loh T, Li X. Hochstereoselektive Synthese von β‐trifluormethylierten Homoallylalkoholen in Wasser Angewandte Chemie. 109: 1029-1031. DOI: 10.1002/Ange.19971090923 |
0.331 |
|
1996 |
Diana SH, Sim K, Loh T. Lanthanum Trifluoromethanesulfonate [La(OTf)3] Promoted Indium-Mediated Coupling of Ethyl 4-Bromocrotonate With Carbonyl Compounds in Water Synlett. 1996: 263-264. DOI: 10.1055/S-1996-5398 |
0.427 |
|
1996 |
Loh T, Pei J, Lin M. Indium trichloride (InCl3) catalysed Diels–Alder reaction in water Chemical Communications. 2315-2316. DOI: 10.1039/Cc9960002315 |
0.545 |
|
1996 |
Loh T, Li X. A versatile and practical synthesis of α-trifluoromethylated alcohols from trifluoroacetaldehyde ethyl hemiacetal in water Chemical Communications. 1929-1930. DOI: 10.1039/Cc9960001929 |
0.358 |
|
1996 |
Loh T, Pei J, Cao G. Indium trichloride catalysed Mukaiyama aldol reaction in water Chemical Communications. 1819-1820. DOI: 10.1039/Cc9960001819 |
0.601 |
|
1996 |
Li X, Loh T. Indium trichloride-promoted tin-mediated carbonyl allylation in water: High simple diastereo- and diastereofacial selectivity Tetrahedron-Asymmetry. 7: 1535-1538. DOI: 10.1016/0957-4166(96)00174-7 |
0.368 |
|
1996 |
Loh T, Wang R, Sim K. Chiral tartrate-derived dioxaborolidine: A simple and practical catalyst for enantioselective Diels-Alder reaction Tetrahedron Letters. 37: 2989-2992. DOI: 10.1016/0040-4039(96)00481-9 |
0.489 |
|
1995 |
Wang R, Lim C, Tan C, Lim B, Sim K, Loh T. Ytterbium trifluoromethanesulfonate [Yb(OTf)3] promoted indium mediated allylation reactions of carbonyl compounds in aqueous media Tetrahedron-Asymmetry. 6: 1825-1828. DOI: 10.1016/0957-4166(95)00228-H |
0.633 |
|
1994 |
Mikami K, Kishino H, Loh T. A unified approach to (22S)- or (22R)-hydroxy steroid side chain: Lewis acid-promoted carbonyl-ene reaction with α-alkoxyaldehydes Journal of the Chemical Society, Chemical Communications. 495-496. DOI: 10.1039/C39940000495 |
0.352 |
|
1994 |
Corey EJ, Guzman-Perez A, Loh T. Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid Journal of the American Chemical Society. 116: 3611-3612. DOI: 10.1021/Ja00087A062 |
0.557 |
|
1993 |
Mikami K, Kishino H, Matsueda H, Loh T. Lactol-Ene Reaction: An Efficient Access to the Synthesis of 22R, 25-Dihydroxy Steroid Side Chains Synlett. 1993: 497-498. DOI: 10.1055/S-1993-22504 |
0.404 |
|
1993 |
Corey E, Loh T. Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products Tetrahedron Letters. 34: 3979-3982. DOI: 10.1016/S0040-4039(00)60594-4 |
0.616 |
|
1992 |
Corey EJ, Loh TP, Sarshar S, Azimioara M. The structure of the 2-methylacrolein boron trifluoride complex in the crystalline phase and in solution Tetrahedron Letters. 33: 6945-6948. DOI: 10.1016/S0040-4039(00)60902-4 |
0.753 |
|
1991 |
Mikami K, Loh T, Nakai T. Acyclic stereocontrol based on nonchelation-controlled ene reactions with α-haloaldehydes Journal of the Chemical Society, Chemical Communications. 77-78. DOI: 10.1039/C39910000077 |
0.434 |
|
1990 |
Mikami K, Kawamoto K, Loh T, Nakai T. Anomalous threo-diastereoselectivity in allylic silane- or stannane–aldehyde condensation reactions: new interpretation of the antiperiplanar vs. synclinal problem on the transition-state conformations Journal of the Chemical Society, Chemical Communications. 1161-1163. DOI: 10.1039/C39900001161 |
0.394 |
|
1990 |
Mikami K, Loh T, Nakai T. Acyclic stereocontrol based on chelation-controlled ene reaction with chiral α- and β-alkoxyaldehydes Tetrahedron: Asymmetry. 1: 13-16. DOI: 10.1016/S0957-4166(00)82265-X |
0.467 |
|
1988 |
Mikami K, Loh T, Nakai T. Ene approach for concurrent control over the chiral centres at C-20 and C-22 of steroid side chains: a highly stereocontrolled synthesis of (20S,22R)-(erythro-)22-hydroxy-23,24-acetylenic steroid side chains Journal of the Chemical Society, Chemical Communications. 1430-1431. DOI: 10.1039/C39880001430 |
0.389 |
|
1988 |
Mikami K, Loh T, Nakai T. Diastereocontrol via Lewis acid-promoted ene reaction with glyoxylates and its application to stereocontrolled synthesis of a 22R-hydroxy-23-carboxylate steroid side chain Tetrahedron Letters. 29: 6305-6308. DOI: 10.1016/S0040-4039(00)82332-1 |
0.441 |
|
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