Year |
Citation |
Score |
2022 |
Kim S, Oiler J, Xing Y, O'Doherty GA. asymmetric Achmatowicz approach to oligosaccharide natural products. Chemical Communications (Cambridge, England). PMID 36321854 DOI: 10.1039/d2cc05280f |
0.684 |
|
2022 |
Wang Y, O'Doherty GA. Synthetic Efforts and Ultimate Limitation to an Asymmetric Achmatowicz Approach Toward EBC-23. The Journal of Organic Chemistry. 87: 6006-6013. PMID 35435679 DOI: 10.1021/acs.joc.2c00262 |
0.37 |
|
2020 |
Dong G, Li B, O'Doherty G. Total and Formal Syntheses of Fostriecin. Organic Chemistry Frontiers : An International Journal of Organic Chemistry. 7: 3608-3615. PMID 33184589 DOI: 10.1039/d0qo01121e |
0.331 |
|
2020 |
Li Y, Seber P, Wright EB, Yasmin S, Lannigan DA, O'Doherty GA. The affinity of RSK for cylitol analogues of SL0101 is critically dependent on the B-ring C-4'-hydroxy. Chemical Communications (Cambridge, England). PMID 32048692 DOI: 10.1039/D0Cc00128G |
0.343 |
|
2020 |
Li Y, Sandusky ZM, Vemula R, Zhang Q, Wu B, Fukuda S, Li M, Lannigan DA, O'Doherty GA. Regioselective Synthesis of a -4'' Carbamate,-6'' -Pr Substituted Cyclitol Analogue of SL0101. Organic Letters. PMID 32009414 DOI: 10.1021/Acs.Orglett.0C00042 |
0.322 |
|
2019 |
Cunha VLS, Liu X, Lowary TL, O'Doherty GA. De Novo Asymmetric Synthesis of Avocadyne, Avocadene and Avocadane Stereoisomers. The Journal of Organic Chemistry. PMID 31647231 DOI: 10.1021/Acs.Joc.9B02391 |
0.418 |
|
2019 |
Gao D, Li B, O'Doherty GA. Synthesis of Dehydro-Dephospho-Fostriecin and Formal Total Synthesis of Fostriecin. Organic Letters. PMID 31584287 DOI: 10.1021/Acs.Orglett.9B03120 |
0.479 |
|
2019 |
Aljahdali AZ, Freedman SA, Scott J, Li M, O'Doherty GA. Synthesis and direct comparison of the anticancer activities of phomopsolides D and E and two 7-oxa-/7-aza-analogues. Medchemcomm. 10: 1205-1211. PMID 31391894 DOI: 10.1039/C9Md00121B |
0.351 |
|
2018 |
Aljahdali AZ, Foster KA, O'Doherty GA. The asymmetric syntheses of cryptocaryols A and B. Chemical Communications (Cambridge, England). PMID 29547218 DOI: 10.1039/C8Cc00482J |
0.385 |
|
2018 |
Aljahdali AZ, Freedman SA, Li M, O'Doherty GA. Asymmetric synthesis of 7-aza-phomopsolide E and its C-4 epimer Tetrahedron. 74: 7121-7126. DOI: 10.1016/J.Tet.2018.10.036 |
0.423 |
|
2018 |
Zhang Q, O'Doherty GA. De novo asymmetric synthesis of (−)-nanaomycin A Tetrahedron. 74: 4994-4999. DOI: 10.1016/J.Tet.2018.06.051 |
0.484 |
|
2017 |
Li M, Li Y, Ludwik KA, Sandusky ZM, Lannigan DA, O'Doherty GA. Stereoselective Synthesis and Evaluation of C6″-Substituted 5a-Carbasugar Analogues of SL0101 as Inhibitors of RSK1/2. Organic Letters. PMID 28441024 DOI: 10.1021/Acs.Orglett.7B00945 |
0.312 |
|
2016 |
Guo H, La Clair JJ, Masler EP, O'Doherty G, Xing Y. De Novo Asymmetric Synthesis and Biological Analysis of the Daumone Pheromones inand in the Soybean Cyst Nematode. Tetrahedron. 72: 2280-2286. PMID 29445247 DOI: 10.1016/J.Tet.2016.03.033 |
0.705 |
|
2016 |
Avocetien KF, Li JJ, Liu X, Wang Y, Xing Y, O'Doherty GA. De Novo Asymmetric Synthesis of Phoracantholide J. Organic Letters. PMID 27635983 DOI: 10.1021/Acs.Orglett.6B02432 |
0.694 |
|
2016 |
Ashmus RA, Jayasuriya AB, Lim YJ, O'Doherty GA, Lowary TL. De novo asymmetric synthesis of a 6-O-methyl-D-glycero-L-gluco-heptopyranose-derived thioglycoside for the preparation of Campylobacter jejuni NCTC11168 capsular polysaccharide fragments. The Journal of Organic Chemistry. PMID 26982173 DOI: 10.1021/Acs.Joc.6B00296 |
0.327 |
|
2016 |
Hunter TJ, Wang Y, Zheng J, O'Doherty GA. Asymmetric Iterative Hydration of Polyene Strategy to Cryptocaryols A and B Synthesis (Germany). 48: 1700-1710. DOI: 10.1055/S-0035-1561607 |
0.35 |
|
2016 |
Hunter TJ, Zheng J, O'Doherty GA. Approach to the synthesis of the C1-C11 and C14-C18 portion of Leucascandrolide A Organic Chemistry Frontiers. 3: 1120-1125. DOI: 10.1039/C6Qo00284F |
0.351 |
|
2016 |
Guo H, La Clair JJ, Masler EP, O'Doherty GA, Xing Y. De novo asymmetric synthesis and biological analysis of the daumone pheromones in Caenorhabditis elegans and in the soybean cyst nematode Heterodera glycines Tetrahedron. 72: 2280-2286. DOI: 10.1016/j.tet.2016.03.033 |
0.68 |
|
2015 |
Ma Y, O'Doherty GA. De Novo Asymmetric Synthesis of (+)-Monanchorin. Organic Letters. 17: 5280-3. PMID 26461800 DOI: 10.1021/Acs.Orglett.5B02651 |
0.409 |
|
2015 |
Huang JL, Wang JZ, Li HX, Guo H, O'Doherty GA. Silylated organometals: A family of recyclable homogeneous catalysts Green Chemistry. 17: 1473-1478. DOI: 10.1039/C4Gc01586J |
0.325 |
|
2015 |
Liu X, Wang Y, O'Doherty GA. The Asymmetric Synthesis of Tetrahydrolipstatin Asian Journal of Organic Chemistry. 4: 994-1009. DOI: 10.1002/Ajoc.201500240 |
0.499 |
|
2015 |
Avocetien K, Li Y, O'Doherty GA. The Alkyne Zipper Reaction in Asymmetric Synthesis Modern Alkyne Chemistry: Catalytic and Atom-Economic Transformations. 365-394. DOI: 10.1002/9783527677894.ch13 |
0.357 |
|
2014 |
Bajaj SO, Sharif EU, Akhmedov NG, O'Doherty GA. De novo asymmetric synthesis of the mezzettiaside family of natural products via the iterative use of a dual B-/Pd-catalyzed glycosylation. Chemical Science (Royal Society of Chemistry : 2010). 5: 2230-2234. PMID 25729559 DOI: 10.1039/C4Sc00593G |
0.453 |
|
2014 |
Bajaj SO, Shi P, Beuning PJ, O'Doherty GA. Structure activity relationship study of Mezzettiasides natural products and their four new disaccharide analogues for anticancer/antibacterial activity. Medchemcomm. 5: 1138-1142. PMID 25729554 DOI: 10.1039/C4Md00095A |
0.32 |
|
2014 |
Mrozowski RM, Sandusky ZM, Vemula R, Wu B, Zhang Q, Lannigan DA, O'Doherty GA. De novo synthesis and biological evaluation of C6″-substituted C4″-amide analogues of SL0101. Organic Letters. 16: 5996-9. PMID 25372628 DOI: 10.1021/Ol503012K |
0.31 |
|
2014 |
Mulzer M, Tiegs BJ, Wang Y, Coates GW, O'Doherty GA. Total synthesis of tetrahydrolipstatin and stereoisomers via a highly regio- and diastereoselective carbonylation of epoxyhomoallylic alcohols. Journal of the American Chemical Society. 136: 10814-20. PMID 25004122 DOI: 10.1021/Ja505639U |
0.373 |
|
2014 |
Sharif EU, Wang HY, Akhmedov NG, O'Doherty GA. Merremoside D: de novo synthesis of the purported structure, NMR analysis, and comparison of spectral data. Organic Letters. 16: 492-5. PMID 24354696 DOI: 10.1021/Ol403369H |
0.39 |
|
2014 |
Kaushik V, Kaulkarni Y, Wright C, O'Doherty G, Azad N, Iyer A. Abstract 3205: Structural analysis of cardiac glycosides to determine the basis for tumoristatic activity Cancer Research. 74: 3205-3205. DOI: 10.1158/1538-7445.Am2014-3205 |
0.366 |
|
2014 |
Bajaj SO, Farnsworth JR, O'Doherty GA. Enantioselective Synthesis of α− and β−Boc-protected 6-Hydroxy-pyranones: Carbohydrate Building Blocks Organic Syntheses. 91: 338-355. DOI: 10.1002/0471264229.Os091.29 |
0.394 |
|
2013 |
Aljahdali AZ, Shi P, Zhong Y, O'Doherty GA. De novo asymmetric synthesis of the pyranoses: from monosaccharides to oligosaccharides. Advances in Carbohydrate Chemistry and Biochemistry. 69: 55-123. PMID 24274368 DOI: 10.1016/B978-0-12-408093-5.00004-6 |
0.421 |
|
2013 |
Wang HY, Guo H, O'Doherty GA. De novo asymmetric synthesis of oligo-rhamno di- and tri-saccharides related to the anthrax tetrasaccharide. Tetrahedron. 69: 3432-3436. PMID 23794755 DOI: 10.1016/J.Tet.2013.02.073 |
0.509 |
|
2013 |
Chen Q, Zhong Y, O'Doherty GA. Convergent de novo synthesis of vineomycinone B2 methyl ester. Chemical Communications (Cambridge, England). 49: 6806-8. PMID 23778961 DOI: 10.1039/C3Cc44050H |
0.424 |
|
2013 |
Hinds JW, McKenna SB, Sharif EU, Wang HY, Akhmedov NG, O'Doherty GA. C3'/C4'-Stereochemical Effects of Digitoxigenin α-L-/α-D-Glycoside in Cancer Cytotoxicity. Chemmedchem. 8: 63-9. PMID 23139074 DOI: 10.1002/Cmdc.201200465 |
0.372 |
|
2013 |
Azad N, Rojanasakul Y, O'Doherty G, Iyer A. Abstract 2265: Antitumorigenic effects of a novel digitoxin analogue. Cancer Research. 73: 2265-2265. DOI: 10.1158/1538-7445.Am2013-2265 |
0.316 |
|
2013 |
Cuccarese MF, Wang HYL, O'Doherty GA. Application of the Wharton rearrangement for the de novo synthesis of pyranosides with ido, manno, and colito stereochemistry European Journal of Organic Chemistry. 3067-3075. DOI: 10.1002/Ejoc.201300051 |
0.478 |
|
2013 |
O'Doherty GA. Carbohydrates-Tools for Stereoselective Synthesis. Edited by Mike Martin Kwabena Boysen. Angewandte Chemie International Edition. 52: 10156-10156. DOI: 10.1002/Anie.201305971 |
0.449 |
|
2013 |
O'Doherty GA. Carbohydrates - Tools for Stereoselective Synthesis. Herausgegeben von Mike Martin Kwabena Boysen. Angewandte Chemie. 125: 10342-10342. DOI: 10.1002/Ange.201305971 |
0.448 |
|
2013 |
Cuccarese MF, O'Doherty GA. Application of the Achmatowicz Rearrangement for the Synthesis of Oligosaccharides Asymmetric Synthesis Ii: More Methods and Applications. 249-259. DOI: 10.1002/9783527652235.ch31 |
0.331 |
|
2012 |
Sharif EU, O'Doherty GA. Biosynthesis and Total Synthesis Studies on The Jadomycin Family of Natural Products. European Journal of Organic Chemistry. 2012. PMID 24371430 DOI: 10.1002/Ejoc.201101609 |
0.393 |
|
2011 |
Yu X, Li M, O'Doherty GA. DE NOVO ASYMMETRIC APPROACH TO THE DISACCHARIDE PORTION OF SCH-47554. Heterocycles. 82: 1577-1584. PMID 29449759 DOI: 10.3987/Com-10-S(E)114 |
0.457 |
|
2011 |
Wang HY, O'Doherty GA. De novo synthesis of deoxy sugar via a Wharton rearrangement. Chemical Communications (Cambridge, England). 47: 10251-3. PMID 21853169 DOI: 10.1039/C1Cc13837E |
0.382 |
|
2011 |
Wang HY, Rojanasakul Y, O'Doherty GA. Synthesis and Evaluation of the α-D-/α-L-Rhamnosyl and Amicetosyl Digitoxigenin Oligomers as Anti-tumor Agents. Acs Medicinal Chemistry Letters. 2: 264-269. PMID 21660118 DOI: 10.1021/Ml100290D |
0.374 |
|
2011 |
Wang HY, Xin W, Zhou M, Stueckle TA, Rojanasakul Y, O'Doherty GA. Stereochemical survey of digitoxin monosaccharides: new anticancer analogues with enhanced apoptotic activity and growth inhibitory effect on human non-small cell lung cancer cell. Acs Medicinal Chemistry Letters. 2: 73-78. PMID 21643465 DOI: 10.1021/Ml100219D |
0.318 |
|
2011 |
Wang HY, Qi Z, Wu B, Kang SW, Rojanasakul Y, O'Doherty GA. C5'-Alkyl Substitution Effects on Digitoxigenin α-l-Glycoside Cancer Cytotoxicity. Acs Medicinal Chemistry Letters. 2: 259-263. PMID 21572583 DOI: 10.1021/Ml100291N |
0.363 |
|
2011 |
Wang Y, Xing Y, Zhang Q, O'Doherty GA. De novo synthesis of natural products via the asymmetric hydration of polyenes. Chemical Communications (Cambridge, England). 47: 8493-505. PMID 21559534 DOI: 10.1039/C1Cc11791B |
0.685 |
|
2010 |
Wu B, Li M, O'Doherty GA. Synthesis of several cleistrioside and cleistetroside natural products via a divergent de novo asymmetric approach. Organic Letters. 12: 5466-9. PMID 21038879 DOI: 10.1021/Ol1023344 |
0.407 |
|
2010 |
Shan M, Sharif EU, O'Doherty GA. Total synthesis of jadomycin A and a carbasugar analogue of jadomycin B. Angewandte Chemie (International Ed. in English). 49: 9492-5. PMID 20979078 DOI: 10.1002/Anie.201005329 |
0.423 |
|
2010 |
Borisova SA, Guppi SR, Kim HJ, Wu B, Penn JH, Liu HW, O'Doherty GA. A de novo approach to the synthesis of glycosylated methymycin analogues with structural and stereochemical diversity. Organic Letters. 12: 5150-3. PMID 20958086 DOI: 10.1021/Ol102144G |
0.415 |
|
2010 |
Gao D, O'Doherty GA. Total synthesis of fostriecin: via a regio- and stereoselective polyene hydration, oxidation, and hydroboration sequence. Organic Letters. 12: 3752-5. PMID 20687585 DOI: 10.1021/Ol101340N |
0.339 |
|
2010 |
Shan M, O'Doherty GA. Synthesis of SL0101 carbasugar analogues: carbasugars via Pd-catalyzed cyclitolization and post-cyclitolization transformations. Organic Letters. 12: 2986-9. PMID 20518547 DOI: 10.1021/Ol101009Q |
0.481 |
|
2010 |
Yu X, Li M, O'Doherty GA. De novo asymmetric approach to the disaccharide portion of SCH-47554 Heterocycles. 82: 1577-1584. DOI: 10.3987/COM-10-S(E)114 |
0.363 |
|
2010 |
Harsh P, O'Doherty GA. ChemInform Abstract: Total Synthesis of Platensimycin and Platencin Cheminform. 41. DOI: 10.1002/CHIN.201016257 |
0.355 |
|
2010 |
Balachari D, Quinn L, O'Doherty GA. ChemInform Abstract: Efficient Synthesis of 5-Aryl-2-vinylfurans by Palladium-Catalyzed Cross-Coupling Strategies. Cheminform. 30: no-no. DOI: 10.1002/chin.199936129 |
0.308 |
|
2010 |
TROST BM, ORGAN MG, O'DOHERTY GA. ChemInform Abstract: Asymmetric Synthesis of Allylic Sulfones. Useful Asymmetric Building Blocks. Cheminform. 27: no-no. DOI: 10.1002/chin.199605088 |
0.487 |
|
2009 |
Shan M, Xing Y, O'Doherty GA. De novo asymmetric synthesis of an alpha-6-deoxyaltropyranoside as well as its 2-/3-deoxy and 2,3-dideoxy congeners. The Journal of Organic Chemistry. 74: 5961-6. PMID 20560564 DOI: 10.1021/Jo9009722 |
0.634 |
|
2009 |
Harsh P, O'Doherty GA. De Novo Asymmetric Syntheses of (+)-Goniothalamin, (+)-Goniothalamin oxide and 7,8-Bis-epi-Goniothalamin using Asymmetric Allylations. Tetrahedron. 65: 5051-5055. PMID 20161297 DOI: 10.1016/J.Tet.2009.03.097 |
0.365 |
|
2009 |
Xing Y, O'Doherty GA. De novo asymmetric synthesis of cladospolide B-D: structural reassignment of cladospolide D via the synthesis of its enantiomer. Organic Letters. 11: 1107-10. PMID 19193044 DOI: 10.1021/Ol9000119 |
0.676 |
|
2009 |
Xing Y, Penn JH, O'Doherty GA. Structure investigations of (ent)-cladospolide d by de novo synthesis and kinetic and thermodynamic isomerization Synthesis. 2847-2854. DOI: 10.1055/S-0029-1217606 |
0.69 |
|
2009 |
Yu X, O'Doherty G. ChemInform Abstract: De novo Synthesis in Carbohydrate Chemistry - From Furans to Monosaccharides and Oligosaccharides Cheminform. 40. DOI: 10.1002/CHIN.200935245 |
0.38 |
|
2009 |
Rajaratnam M, O'Doherty GA. Total synthesis of sceptrin and dibromosceptrin Chemtracts. 22: 59-66. |
0.365 |
|
2009 |
Wang HYL, O'Doherty GA. Stereocontrolled synthesis of pentacyclic core in ecteinascidin 743 Chemtracts. 22: 96-111. |
0.316 |
|
2009 |
Mingde S, Leo W, Qi Z, O'Doherty GA. Tactics in total synthesis of (-)-kendomycin Chemtracts. 22: 1-17. |
0.365 |
|
2009 |
Niu D, Yan W, Sharif E, Rajaratnam M, O'Doherty GA. Total synthesis of (-)-cephalotaxine Chemtracts. 22: 89-95. |
0.365 |
|
2008 |
Guo H, O'Doherty GA. De novo asymmetric synthesis of anthrax tetrasaccharide and related tetrasaccharide. The Journal of Organic Chemistry. 73: 5211-20. PMID 18563936 DOI: 10.1021/Jo800691V |
0.402 |
|
2008 |
Guo H, Mortensen MS, O'Doherty GA. Formal total synthesis of RK-397 via an asymmetric hydration and iterative allylation strategy. Organic Letters. 10: 3149-52. PMID 18549226 DOI: 10.1021/Ol801055B |
0.432 |
|
2008 |
Zhou M, O'Doherty GA. De novo synthesis of the trisaccharide subunit of landomycins A and E. Organic Letters. 10: 2283-6. PMID 18461951 DOI: 10.1021/Ol800697K |
0.345 |
|
2008 |
Baiga TJ, Guo H, Xing Y, O'Doherty GA, Dillin A, Austin MB, Noel JP, La Clair JJ. Metabolite induction of Caenorhabditis elegans dauer larvae arises via transport in the pharynx. Acs Chemical Biology. 3: 294-304. PMID 18376812 DOI: 10.1021/Cb700269E |
0.588 |
|
2008 |
Zhou M, O'Doherty G. The de novo synthesis of oligosaccharides: application to the medicinal chemistry SAR-study of digitoxin. Current Topics in Medicinal Chemistry. 8: 114-25. PMID 18289081 DOI: 10.2174/156802608783378828 |
0.468 |
|
2008 |
Guo H, O'Doherty GA. De Novo Asymmetric Syntheses of d-, l- and 8-epi-Swainsonine. Tetrahedron. 64: 304-313. PMID 18283329 DOI: 10.1016/J.Tet.2007.10.109 |
0.478 |
|
2008 |
Abrams JN, Babu RS, Guo H, Le D, Le J, Osbourn JM, O'Doherty GA. De novo asymmetric synthesis of 8a-epi-swainsonine. The Journal of Organic Chemistry. 73: 1935-40. PMID 18237188 DOI: 10.1021/Jo702476Q |
0.486 |
|
2008 |
Zhou M, O'Doherty G. ChemInform Abstract: De novo Synthesis of Oligosaccharides - Application to the Medicinal Chemistry SAR Study of Digitoxin Cheminform. 39. DOI: 10.1002/CHIN.200827246 |
0.306 |
|
2007 |
Mortensen MS, Osbourn JM, O'Doherty GA. De novo formal synthesis of (-)-virginiamycin M2 via the asymmetric hydration of dienoates. Organic Letters. 9: 3105-8. PMID 17608433 DOI: 10.1021/Ol071145E |
0.387 |
|
2007 |
Guo H, O'Doherty GA. De novo asymmetric synthesis of the anthrax tetrasaccharide by a palladium-catalyzed glycosylation reaction. Angewandte Chemie (International Ed. in English). 46: 5206-8. PMID 17534991 DOI: 10.1002/Anie.200701354 |
0.493 |
|
2007 |
Guppi SR, O'Doherty GA. Synthesis of aza-analogues of the glycosylated tyrosine portion of mannopeptimycin-E. The Journal of Organic Chemistry. 72: 4966-9. PMID 17530803 DOI: 10.1021/Jo070326R |
0.483 |
|
2007 |
Zhou M, O'Doherty GA. De novo approach to 2-deoxy-beta-glycosides: asymmetric syntheses of digoxose and digitoxin. The Journal of Organic Chemistry. 72: 2485-93. PMID 17338573 DOI: 10.1021/Jo062534+ |
0.37 |
|
2006 |
Li M, O'Doherty GA. De novo formal synthesis of (-)-apicularen A via an iterative asymmetric hydration sequence. Organic Letters. 8: 6087-90. PMID 17165936 DOI: 10.1021/Ol062595U |
0.42 |
|
2006 |
Shan M, O'Doherty GA. De novo asymmetric syntheses of SL0101 and its analogues via a palladium-catalyzed glycosylation. Organic Letters. 8: 5149-52. PMID 17048865 DOI: 10.1021/Ol062076R |
0.394 |
|
2006 |
Ahmed MM, Mortensen MS, O'Doherty GA. De novo synthesis of 2-substituted syn-1,3-diols via an iterative asymmetric hydration strategy. The Journal of Organic Chemistry. 71: 7741-6. PMID 16995681 DOI: 10.1021/Jo061200H |
0.463 |
|
2006 |
Zhou M, O'Doherty GA. A stereoselective synthesis of digitoxin and digitoxigen mono- and bisdigitoxoside from digitoxigenin via a palladium-catalyzed glycosylation. Organic Letters. 8: 4339-42. PMID 16956221 DOI: 10.1021/Ol061683B |
0.401 |
|
2006 |
Li M, O'Doherty GA. De novo asymmetric synthesis of milbemycin beta3 via an iterative asymmetric hydration approach. Organic Letters. 8: 3987-90. PMID 16928055 DOI: 10.1021/Ol061439K |
0.415 |
|
2006 |
Ahmed MM, Cui H, O'Doherty GA. De novo asymmetric syntheses of muricatacin and its analogues via dihydroxylation of dienoates. The Journal of Organic Chemistry. 71: 6686-9. PMID 16901173 DOI: 10.1021/Jo061057S |
0.482 |
|
2006 |
Ahmed MM, O'Doherty GA. De novo asymmetric syntheses of C-4-substituted sugars via an iterative dihydroxylation strategy. Carbohydrate Research. 341: 1505-21. PMID 16616898 DOI: 10.1016/J.Carres.2006.03.024 |
0.354 |
|
2006 |
Guo H, O'Doherty GA. De novo asymmetric synthesis of D- and L-swainsonine. Organic Letters. 8: 1609-12. PMID 16597122 DOI: 10.1021/Ol0602811 |
0.506 |
|
2006 |
Guppi SR, Zhou M, O'Doherty GA. De novo asymmetric synthesis of homoadenosine via a palladium-catalyzed N-glycosylation. Organic Letters. 8: 293-6. PMID 16408898 DOI: 10.1021/Ol052664P |
0.474 |
|
2006 |
Mortensen MS, Schmitt AC, Smith CM, Voight EA, O'Doherty GA. A diastereoselective silver(I) promoted Gem-dibromocyclopropane ring opening reaction via an anchimeric assisted transannular benzoate migration Heterocycles. 67: 721-730. DOI: 10.3987/Com-05-S(T)69 |
0.457 |
|
2006 |
Ahmed MM, Akhmedov NG, Cui H, Friedrich D, O'Doherty GA. A de novo asymmetric approach to achiral deoxy-melodorinol analogues Heterocycles. 70: 223-233. DOI: 10.1002/Chin.200722214 |
0.489 |
|
2006 |
O'Doherty GA, Zhou M. Stereocontrolled Total Synthesis of (+)-Streptazolin Cheminform. 37. DOI: 10.1002/chin.200610266 |
0.375 |
|
2005 |
Ahmed MM, O'Doherty GA. De novo asymmetric syntheses of D- and L-talose via an iterative dihydroxylation of dienoates. The Journal of Organic Chemistry. 70: 10576-8. PMID 16323875 DOI: 10.1021/Jo051476+ |
0.355 |
|
2005 |
Gao D, O'Doherty GA. De novo asymmetric synthesis of anamarine and its analogues. The Journal of Organic Chemistry. 70: 9932-9. PMID 16292824 DOI: 10.1021/Jo051681P |
0.495 |
|
2005 |
Guo H, O'doherty GA. de novo asymmetric synthesis of daumone via a palladium-catalyzed glycosylation. Organic Letters. 7: 3921-4. PMID 16119932 DOI: 10.1021/Ol051383E |
0.51 |
|
2005 |
Rose MW, Xu J, Kale TA, O'Doherty G, Barany G, Distefano MD. Enzymatic incorporation of orthogonally reactive prenylazide groups into peptides using geranylazide diphosphate via protein farnesyltransferase: implications for selective protein labeling. Biopolymers. 80: 164-71. PMID 15810014 DOI: 10.1002/Bip.20239 |
0.316 |
|
2005 |
Gao D, O'Doherty GA. Enantioselective synthesis of 10-epi-anamarine via an iterative dihydroxylation sequence. Organic Letters. 7: 1069-72. PMID 15760141 DOI: 10.1021/Ol047322I |
0.455 |
|
2005 |
Ahmed MM, Berry BP, Hunter TJ, Tomcik DJ, O'Doherty GA. De novo enantioselective syntheses of galacto-sugars and deoxy sugars via the iterative dihydroxylation of dienoate. Organic Letters. 7: 745-8. PMID 15704940 DOI: 10.1021/Ol050044I |
0.438 |
|
2005 |
Babu RS, O'Doherty GA. Palladium-catalyzed glycosylation reaction: De-Novo synthesis of trehalose analogues Journal of Carbohydrate Chemistry. 24: 169-177. DOI: 10.1081/Car-200059959 |
0.455 |
|
2005 |
Zhang Y, O'Doherty GA. Remote steric effect on the regioselectivity of Sharpless asymmetric dihydroxylation Tetrahedron. 61: 6337-6351. DOI: 10.1016/J.Tet.2005.03.119 |
0.325 |
|
2004 |
Babu RS, Zhou M, O'Doherty GA. De novo synthesis of oligosaccharides using a palladium-catalyzed glycosylation reaction. Journal of the American Chemical Society. 126: 3428-9. PMID 15025462 DOI: 10.1021/Ja039400N |
0.462 |
|
2004 |
Schmitt AC, Smith CM, Voight EA, O'Doherty GA. Facial selectivity of the sharpless bromine catalyzed aziridination Heterocycles. 62: 635-642. DOI: 10.3987/Com-03-S(P)57 |
0.417 |
|
2004 |
Harris JM, Li M, Scott JG, O'Doherty GA. Chapter 8 Achmatowicz approach to 5,6-dihydro-2H-pyran-2-one containing natural products Strategies and Tactics in Organic Synthesis. 5: 221-253. DOI: 10.1016/S1874-6004(04)80031-5 |
0.458 |
|
2004 |
Li M, O'Doherty GA. An enantioselective synthesis of phomopsolide D Tetrahedron Letters. 45: 6407-6411. DOI: 10.1016/J.Tetlet.2004.07.011 |
0.332 |
|
2003 |
Babu RS, O'Doherty GA. A palladium-catalyzed glycosylation reaction: the de novo synthesis of natural and unnatural glycosides. Journal of the American Chemical Society. 125: 12406-7. PMID 14531673 DOI: 10.1021/Ja037097K |
0.416 |
|
2003 |
Smith CM, O'Doherty GA. Enantioselective syntheses of cryptocarya triacetate, cryptocaryolone, and cryptocaryolone diacetate. Organic Letters. 5: 1959-62. PMID 12762696 DOI: 10.1021/Ol0345529 |
0.499 |
|
2002 |
Hunter TJ, O'Doherty GA. Enantioselective syntheses of colletodiol, colletol, and grahamimycin A. Organic Letters. 4: 4447-50. PMID 12465909 DOI: 10.1021/Ol0269502 |
0.487 |
|
2002 |
Haukaas MH, O'Doherty GA. Enantioselective synthesis of 2-deoxy- and 2,3-dideoxyhexoses. Organic Letters. 4: 1771-4. PMID 12000295 DOI: 10.1021/Ol025844X |
0.467 |
|
2002 |
Garaas SD, Hunter TJ, O'Doherty GA. An enantioselective synthesis of tarchonanthuslactone. The Journal of Organic Chemistry. 67: 2682-5. PMID 11950317 DOI: 10.1021/Jo0163400 |
0.531 |
|
2002 |
Harris JM, O'Doherty GA. An enantioselective total synthesis of phomopsolide C Tetrahedron Letters. 43: 8195-8199. DOI: 10.1016/S0040-4039(02)01866-X |
0.43 |
|
2001 |
Haukaas MH, O'Doherty GA. Enantioselective synthesis of N-Cbz-protected 6-amino-6-deoxymannose, -talose, and -gulose Organic Letters. 3: 3899-3902. PMID 11720564 DOI: 10.1021/Ol016743M |
0.462 |
|
2001 |
Hunter TJ, O'Doherty GA. An enantioselective synthesis of cryptocarya diacetate Organic Letters. 3: 2777-2779. PMID 11506632 DOI: 10.1021/Ol016399T |
0.515 |
|
2001 |
Haukaas MH, O'Doherty GA. Synthesis of D- and L-Deoxymannojirimycin via an Asymmetric Aminohydroxylation of Vinylfuran Organic Letters. 3: 401-404. PMID 11428024 DOI: 10.1021/Ol006907J |
0.414 |
|
2001 |
Hunter TJ, O'Doherty GA. An enantioselective synthesis of benzylidene-protected syn-3,5-dihydroxy carboxylate esters via osmium, palladium, and base catalysis Organic Letters. 3: 1049-1052. PMID 11277792 DOI: 10.1021/Ol0156188 |
0.492 |
|
2001 |
Harris JM, O'Doherty GA. An olefination approach to the enantioselective syntheses of several styryllactones Tetrahedron. 57: 5161-5171. DOI: 10.1016/S0040-4020(01)00355-6 |
0.438 |
|
2000 |
Balachari D, O'Doherty GA. Enantioselective synthesis of the papulacandin ring system: Conversion of the mannose diastereoisomer into a glucose stereoisomer Organic Letters. 2: 4033-4036. PMID 11112636 DOI: 10.1021/Ol006662A |
0.422 |
|
2000 |
Harris JM, Keränen MD, Nguyen H, Young VG, O'Doherty GA. Syntheses of four D- and L-hoxoses via diastereoselective and enantioselective dihydroxylation reactions Carbohydrate Research. 328: 17-36. PMID 11005573 DOI: 10.1016/S0008-6215(00)00031-8 |
0.434 |
|
2000 |
Harris JM, O'Doherty GA. Enantioselective syntheses of isoaltholactone, 3-epi-altholactone, and 5-hydroxygoniothalamin Organic Letters. 2: 2983-2986. PMID 10986088 DOI: 10.1021/Ol000179I |
0.396 |
|
2000 |
Balachari D, O'Doherty GA. Sharpless asymmetric dihydroxylation of 5-aryl-2-vinylfurans: Application to the synthesis of the spiroketal moiety of papulacandin D Organic Letters. 2: 863-866. PMID 10754689 DOI: 10.1021/Ol0000253 |
0.513 |
|
2000 |
Harris JM, O'Doherty GA. Enantioselective synthesis of 5-substituted α,β-unsaturated δ- lactones: Application to the synthesis of styryllactones Tetrahedron Letters. 41: 183-187. |
0.347 |
|
1999 |
Bushey ML, Haukaas MH, O'Doherty GA. Asymmetric Aminohydroxylation of Vinylfuran. The Journal of Organic Chemistry. 64: 2984-2985. PMID 11674385 DOI: 10.1021/Jo990095R |
0.388 |
|
1999 |
Harris JM, Keranen MD, O'Doherty GA. Syntheses of D- and L-Mannose, Gulose, and Talose via Diastereoselective and Enantioselective Dihydroxylation Reactions. The Journal of Organic Chemistry. 64: 2982-2983. PMID 11674384 DOI: 10.1021/Jo990410+ |
0.38 |
|
1999 |
Balachari D, Quinn L, O'Doherty GA. Efficient synthesis of 5-aryl-2-vinylfurans by palladium catalyzed cross-coupling strategies Tetrahedron Letters. 40: 4769-4773. DOI: 10.1016/S0040-4039(99)00817-5 |
0.448 |
|
1995 |
Trost BM, Organ MG, O'Doherty GA. Asymmetric synthesis of allylic sulfones useful as asymmetric building blocks. Journal of the American Chemical Society. 117: 9662-9670. DOI: 10.1021/Ja00143A007 |
0.673 |
|
1995 |
Trost BM, Organ MG, O'Doherty GA. Asymmetric synthesis of allylic sulfones. Useful asymmetric building blocks Journal of the American Chemical Society. 117: 9662-9670. |
0.61 |
|
1994 |
Houk KN, Li Y, McAllister MA, O'Doherty G, Paquette LA, Siebrand W, Smedarchina ZK. Mechanistic Analysis of Double Hydrogen Dyotropy in syn-Sesquinorbornene Disulfones. A Combined Kinetic and Theoretical Evaluation of Primary Deuterium Isotope Effects Journal of the American Chemical Society. 116: 10895-10913. DOI: 10.1021/Ja00103A005 |
0.377 |
|
1994 |
O'Doherty GA, Rogers RD, Paquette LA. Consequences of Modulated Precompression along Reaction Coordinates. Synthesis, Crystallographic Structural Studies, and Rate of Intramolecular Dyotropy in an Extended Series of syn-Sesquinorbornene Disulfones Journal of the American Chemical Society. 116: 10883-10894. DOI: 10.1021/Ja00103A004 |
0.521 |
|
1991 |
Sornay C, Meunier P, Gautheron B, O'Doherty GA, Paquette LA. Isodicyclopentadienes and related molecules. Part 54. Stereoselective access to the three diisodicyclopentadienyltitanium dichlorides Organometallics. 10: 2082-2083. DOI: 10.1021/Om00052A068 |
0.332 |
|
1991 |
Paquette LA, O'Doherty GA, Rogers RD. Intramolecular reaction rate is not determined exclusively by the distance separating reaction centers. The kinetic consequences of modulated ground state strain on dyotropic hydrogen migration in systems of very similar geometric disposition [Erratum to document cited in CA115(17):182353r] Journal of the American Chemical Society. 113: 9710-9710. DOI: 10.1021/Ja00025A067 |
0.42 |
|
1991 |
Paquette LA, O'Doherty GA, Rogers RD. Intramolecular reaction rate is not determined exclusively by the distance separating reaction centers. The kinetic consequences of modulated ground state strain on dyotropic hydrogen migration in systems of very similar geometric disposition Journal of the American Chemical Society. 113: 7761-7762. DOI: 10.1021/Ja00020A048 |
0.429 |
|
1991 |
Bauer W, O'Doherty GA, Schleyer PvR, Paquette LA. Isodicyclopentadienes and related molecules. 58. Structural analysis of a camphor-derived cyclopentadienyllithium compound by NMR and MNDO. A ternary equilibrium in tetrahydrofuran Journal of the American Chemical Society. 113: 7093-7100. DOI: 10.1021/Ja00019A001 |
0.403 |
|
1989 |
Paquette LA, O'Doherty GA, Miller BL, Rogers RD, Rheingold AL, Geib SL. Isodicyclopentadienes and related molecules. 48. Stereochemically uniform mode of iron carbonyl complexation to spirocyclic isodicyclopentadienes Organometallics. 8: 2167-2172. DOI: 10.1021/Om00111A012 |
0.346 |
|
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