Year |
Citation |
Score |
2023 |
Kesavulu G, Balachandra B, Prasad KR. Lithio Tris(methylthio)methane as Hydroxy/Thio/Aminocarbonyl Anion Equivalent: Asymmetric Synthesis of α-Amino Acid Esters, Thioesters, Amides, and Peptides. Organic Letters. 25: 5168-5172. PMID 37406168 DOI: 10.1021/acs.orglett.3c01969 |
0.444 |
|
2023 |
Silambarasan K, Kesavulu G, Reddy AA, Prasad KR. Diastereoselective Synthesis of -β-Amino Cyclohexyl Ketones and -3-Amino-4-acyl-tetrahydropyrans from Intramolecular C-Alkylation of ω-Halo-Substituted β-Sulfinamido Ketones. The Journal of Organic Chemistry. 88: 2006-2022. PMID 36753743 DOI: 10.1021/acs.joc.2c02227 |
0.442 |
|
2021 |
Khandare SP, Prasad KR. Four-Step Total Synthesis of (+)-Euphococcinine and (±)-Adaline. The Journal of Organic Chemistry. PMID 34410729 DOI: 10.1021/acs.joc.1c00938 |
0.502 |
|
2021 |
Nanda LN, Shruthi KS, Prasad KR. γ-Hydroxy Amides from Tartaric Acid: Versatile Chiral Building Blocks for the Total Synthesis of Natural Products. Chemical Record (New York, N.Y.). PMID 34212498 DOI: 10.1002/tcr.202100129 |
0.834 |
|
2020 |
Khandare SP, Reddy PO, Prasad KR. Addition of Lithium Anion of (Acetylmethylene)triphenylphosphorane to Nonracemic Sulfinimines: Total Synthesis of (+)-241D and Formal Total Synthesis of (+)-Preussin. Organic Letters. PMID 32852218 DOI: 10.1021/Acs.Orglett.0C02608 |
0.606 |
|
2020 |
Reddy PO, Reddy AA, Prasad KR. Stereoselective Synthesis of β-Amino Ynones by Addition of Alkynones to Non-racemic Sulfinimines: Formal Total Synthesis of L-Xylo and L-Arabino Phytosphingosines. The Journal of Organic Chemistry. PMID 31913627 DOI: 10.1021/Acs.Joc.9B02938 |
0.53 |
|
2019 |
Uphade MB, Reddy AA, Khandare SP, Prasad KR. Stereoselective Addition of a Lithium Anion of 1,1-Diphenyl-2-aza-pentadiene to Sulfinimines: Application to the Synthesis of (-)-Epiquinamide. Organic Letters. PMID 31691559 DOI: 10.1021/Acs.Orglett.9B03507 |
0.499 |
|
2019 |
Airan Y, Prasad KR. Furan Oxidation Strategy for the Synthesis of the Macrolactone Analogue of Migrastatin. The Journal of Organic Chemistry. PMID 31615208 DOI: 10.1021/Acs.Joc.9B02413 |
0.499 |
|
2019 |
Prasad KR, Uphade MB. Stereoselective Conjugate Addition of the Lithium Anion of N-Allyl Imine to Unsaturated Esters: Application to the Enantiospecific Total Synthesis of (-)-Epibatidine. The Journal of Organic Chemistry. PMID 31293165 DOI: 10.1021/Acs.Joc.9B01340 |
0.543 |
|
2019 |
Prasad KR, Rangari VA. Stereoselective addition of Grignard reagents to sulfinimines derived from tartrate diol (threitol): Generation of chiral building blocks for the collective total synthesis of lentiginosine, conhydrine and methyldihydropalustramate Tetrahedron. 75: 130496. DOI: 10.1016/J.Tet.2019.130496 |
0.632 |
|
2018 |
Reddy AA, Prasad KR. Addition of Lithium Anion of Diphenylmethanol Methyl/ MOM Ether to Non-racemic Sulfinimines: Two Step Asymmetric Synthesis of Diphenylprolinol Methyl Ether and Chiral Diphenylmethoxymethyl Amines. The Journal of Organic Chemistry. PMID 30129765 DOI: 10.1021/Acs.Joc.8B01381 |
0.529 |
|
2018 |
Prasad KR, Rangari VA. Efficient enantiospecific synthesis of ent-conduramine F-1 Tetrahedron. 74: 6689-6693. DOI: 10.1016/J.Tet.2018.09.058 |
0.587 |
|
2018 |
Vaithegi K, Prasad KR. Total Synthesis of Sch 725674 Tetrahedron. 74: 2488-2492. DOI: 10.1016/J.Tet.2018.04.014 |
0.506 |
|
2018 |
Vaithegi K, Prasad KR. Enantiospecific total synthesis of the putative structure of cryptopyranmoscatone B2 Tetrahedron. 74: 2627-2633. DOI: 10.1016/J.Tet.2018.04.011 |
0.526 |
|
2017 |
Reddy AA, Prasad KR. Synthesis of β-Amino Ketones by Addition of Aryl Methyl Ketones to Sulfinimines: Application to the Total Synthesis of HPA-12, Norsedamine and Sedamine. The Journal of Organic Chemistry. PMID 29160073 DOI: 10.1021/Acs.Joc.7B02611 |
0.584 |
|
2016 |
Revu O, Prasad KR. Total Synthesis of the Bis-silyl Ether of (+)-15-epi-Aetheramide A. The Journal of Organic Chemistry. PMID 27936701 DOI: 10.1021/Acs.Joc.6B02535 |
0.389 |
|
2016 |
Reddy AA, Reddy PO, Prasad KR. Synthesis of beta-Amino Substitued Enones by Addition of Substituted Methyl Enones to Sulfinimines: Application to the Total Synthesis of alkaloids (+)-Lasubine II, (+)-241D and Formal Total Synthesis of (-)-Lasubine I. The Journal of Organic Chemistry. PMID 27732001 DOI: 10.1021/Acs.Joc.6B01541 |
0.531 |
|
2016 |
Bali AK, Sunnam SK, Prasad KR. Enantiospecific synthesis of functionalized polyols from tartaric acid using Ley's dithiaketalization: Application to the total synthesis of achaetolide Tetrahedron. 72: 8623-8636. DOI: 10.1016/J.Tet.2016.11.035 |
0.652 |
|
2016 |
Revu O, Uphade MB, Prasad KR. Synthesis and evaluation of C2-symmetric bis-sulfinamides as effective ligands in rhodium catalyzed addition of arylboronic acids to cycloalkenones Tetrahedron. 72: 5355-5362. DOI: 10.1016/J.Tet.2016.07.024 |
0.509 |
|
2015 |
Nagaraju C, Prasad KR. Gold catalyzed intramolecular hydroalkoxylation assisted ring opening of furans to the corresponding saturated γ-keto esters Tetrahedron. 71: 9081-9087. DOI: 10.1016/J.Tet.2015.10.017 |
0.461 |
|
2014 |
Kumar SM, Prasad KR. Enantiospecific formal total synthesis of iriomoteolide 3a. Chemistry, An Asian Journal. 9: 3431-9. PMID 25234434 DOI: 10.1002/Asia.201402593 |
0.581 |
|
2014 |
Nagaraju C, Prasad KR. An unusual ring-contraction/rearrangement sequence for making functionalized di- and triquinanes. Angewandte Chemie (International Ed. in English). 53: 10997-1000. PMID 25163804 DOI: 10.1002/Anie.201407680 |
0.495 |
|
2014 |
Bali AK, Sunnam SK, Prasad KR. Enantiospecific total synthesis of macrolactone Sch 725674. Organic Letters. 16: 4001-3. PMID 25033232 DOI: 10.1021/Ol5018678 |
0.657 |
|
2014 |
Prasad KR, Revu O. Total synthesis of (+)-seimatopolide A. The Journal of Organic Chemistry. 79: 1461-6. PMID 24392655 DOI: 10.1021/Jo4023827 |
0.512 |
|
2014 |
Revu O, Prasad KR. An expeditious asymmetric synthesis of the polyketide unit present in HIV-inhibitory depsipeptides aetheramide A and B Synlett. 25: 2887-2890. DOI: 10.1055/S-0034-1379476 |
0.384 |
|
2014 |
Nidhiry JE, Prasad KR. Synthesis of azepino[4,5- b ]indolones by an intramolecular cyclization of unsaturated tryptamides Synlett. 25: 2585-2590. DOI: 10.1055/S-0034-1379083 |
0.587 |
|
2014 |
Prasad KR, Nidhiry JE, Sridharan M. Total synthesis of the indole alkaloids henrycinol A and B Tetrahedron. 70: 4611-4616. DOI: 10.1016/J.Tet.2014.05.028 |
0.555 |
|
2014 |
Prasad KR, Mothish Kumar S. Total synthesis of (+)-anamarine Tetrahedron. 70: 4552-4556. DOI: 10.1016/J.Tet.2014.04.068 |
0.635 |
|
2014 |
Sunnam SK, Prasad KR. Enantioselective synthesis of macrolactone core of the natural product Sch725674 Tetrahedron. 70: 2096-2101. DOI: 10.1016/J.Tet.2014.02.008 |
0.526 |
|
2014 |
Prasad KR, Nidhiry JE, Sridharan M. ChemInform Abstract: Total Synthesis of the Indole Alkaloids Henrycinol A (Ia) and B (Ib). Cheminform. 45: no-no. DOI: 10.1002/chin.201451206 |
0.349 |
|
2014 |
Prasad KR, Mothish Kumar S. ChemInform Abstract: Total Synthesis of (+)-Anamarine. Cheminform. 45: no-no. DOI: 10.1002/chin.201450200 |
0.47 |
|
2013 |
Prasad KR, Nagaraju C. Facile synthesis of isochromanones and isoquinolones by AuCl3 catalyzed cascade triggered by an internal nucleophile. Organic Letters. 15: 2778-81. PMID 23701587 DOI: 10.1021/Ol4011129 |
0.598 |
|
2013 |
Reddy CR, Jithender E, Prasad KR. Total syntheses of the proposed structure for ieodoglucomides A and B Journal of Organic Chemistry. 78: 4251-4260. PMID 23565942 DOI: 10.1021/jo400041p |
0.36 |
|
2013 |
Prasad KR, Gutala P. Total synthesis and determination of the absolute configuration of 5,6-dihydro-α-pyrone natural product synargentolide B. The Journal of Organic Chemistry. 78: 3313-22. PMID 23477705 DOI: 10.1021/Jo400083V |
0.5 |
|
2013 |
Metri PK, Schiess R, Prasad KR. Enantiospecific total synthesis of (-)-bengamide E. Chemistry, An Asian Journal. 8: 488-93. PMID 23208822 DOI: 10.1002/Asia.201200999 |
0.592 |
|
2013 |
Sunnam SK, Prasad KR. Total synthesis of (+)-pinellic acid Synthesis (Germany). 45: 1991-1996. DOI: 10.1055/S-0033-1338799 |
0.634 |
|
2013 |
Prasad KR, Kumar SM. An expeditious enantiospecific total synthesis of (-)-crassalactone C Synthesis (Germany). 45: 785-790. DOI: 10.1055/S-0032-1318303 |
0.591 |
|
2013 |
Venkanna A, Sreedhar E, Siva B, Babu KS, Prasad KR, Rao JM. Studies directed towards the total synthesis of koshikalide: Stereoselective synthesis of the macrocyclic core Tetrahedron Asymmetry. 24: 1010-1022. DOI: 10.1016/j.tetasy.2013.07.002 |
0.552 |
|
2013 |
Prasad KR, Revu O. 2-Pyridylsulfinamides as effective catalysts in the asymmetric alkylation of aldehydes with diethylzinc Dedicated to Dr. N.N. Joshi, National Chemical Laboratory, Pune, India Tetrahedron. 69: 8422-8428. DOI: 10.1016/J.Tet.2013.07.061 |
0.426 |
|
2013 |
Prasad KR, Kumar SM. Unprecedented formation of a 14-membered dihydropyran macrocycle via sequential olefin cross metathesis-intramolecular hetero Diels-Alder reaction Tetrahedron. 69: 6512-6518. DOI: 10.1016/J.Tet.2013.05.032 |
0.468 |
|
2013 |
Nidhiry JE, Prasad KR. Enantiospecific total synthesis of indole alkaloids (+)-eburnamonine, (-)-aspidospermidine and (-)-quebrachamine Tetrahedron. 69: 5525-5536. DOI: 10.1016/J.Tet.2013.04.097 |
0.609 |
|
2012 |
Pawar AB, Prasad KR. Formal total synthesis of palmerolide A. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15202-6. PMID 23033158 DOI: 10.1002/Chem.201202324 |
0.667 |
|
2012 |
Prasad KR, Revu O. Total Synthesis of (+)-Cladospolide A Synthesis. 44: 2243-2248. DOI: 10.1055/S-0031-1291154 |
0.559 |
|
2012 |
Prasad KR, Nidhiry JE. Total Synthesis of (+)-Eburnamonine Synlett. 23: 1477-1480. DOI: 10.1055/S-0031-1291143 |
0.596 |
|
2012 |
Prasad KR, Gutala P. Total synthesis of (+)-phomopsolide B Tetrahedron. 68: 7489-7493. DOI: 10.1016/J.Tet.2012.06.002 |
0.521 |
|
2011 |
Prasad KR, Pawar AB. Enantioselective formal synthesis of palmerolide A. Organic Letters. 13: 4252-5. PMID 21793548 DOI: 10.1021/Ol201604C |
0.587 |
|
2011 |
Prasad KR, Penchalaiah K. Total synthesis of (-)-anamarine. The Journal of Organic Chemistry. 76: 6889-93. PMID 21739986 DOI: 10.1021/Jo2010389 |
0.633 |
|
2011 |
Prasad KR, Swain B. Enantioselective synthesis of possible diastereomers of heptadeca-1-ene-4,6-diyne-3,8,9,10-tetrol; putative structure of a conjugated diyne natural product isolated from Hydrocotyle leucocephala. The Journal of Organic Chemistry. 76: 2029-39. PMID 21384868 DOI: 10.1021/Jo102201K |
0.408 |
|
2011 |
Prasad KR, Kumar SM. Total Synthesis of Gabosine H Synlett. 2011: 1602-1604. DOI: 10.1055/S-0030-1260782 |
0.531 |
|
2011 |
Prasad KR, Penchalaiah K. Total synthesis of (−)-ent-pachastrissamine (ent-Jaspine B) Tetrahedron-Asymmetry. 22: 1400-1403. DOI: 10.1016/J.Tetasy.2011.07.010 |
0.558 |
|
2011 |
Prasad KR, Swain B. Total synthesis of panaxytriol and panaxydiol Tetrahedron-Asymmetry. 22: 1261-1265. DOI: 10.1016/J.Tetasy.2011.07.007 |
0.642 |
|
2011 |
Prasad KR, Gandi VR. Enantioselective total synthesis of iso-cladospolide B, cladospolide C and cladospolide B from tartaric acid Tetrahedron-Asymmetry. 22: 499-505. DOI: 10.1016/J.Tetasy.2011.02.018 |
0.528 |
|
2011 |
Prasad KR, Gutala P. Enantioselective total synthesis of macrosphelides A and E Tetrahedron. 67: 4514-4520. DOI: 10.1016/J.Tet.2011.04.099 |
0.603 |
|
2011 |
Prasad KR, Penchalaiah K. Enantiodivergent total synthesis of microcarpalide from l-tartaric acid Tetrahedron. 67: 4268-4276. DOI: 10.1016/J.Tet.2011.03.102 |
0.609 |
|
2010 |
Prasad KR, Pawar AB. Stereoselective Synthesis of C1-C18 Region of Palmerolide A from Tartaric Acid Synlett. 2010: 1093-1095. DOI: 10.1055/S-0029-1219797 |
0.512 |
|
2010 |
Prasad KR, Gandi VR, Nidhiry JE, Bhat KS. Enantiodivergent formal total synthesis of aspercyclide C from l -(+)-tartaric acid Synthesis. 2521-2526. DOI: 10.1055/S-0029-1218831 |
0.524 |
|
2010 |
Prasad KR, Gandi VR. Formal total synthesis of (+)-didemniserinolipid B Tetrahedron-Asymmetry. 21: 2848-2852. DOI: 10.1016/J.Tetasy.2010.11.006 |
0.625 |
|
2010 |
Prasad KR, Penchalaiah K. Stereoselective total synthesis of (+)-synargentolide A Tetrahedron-Asymmetry. 21: 2853-2858. DOI: 10.1016/J.Tetasy.2010.11.005 |
0.656 |
|
2010 |
Prasad KR, Gandi VR. Facile enantiospecific synthesis of (+)-iso-cladospolide B Tetrahedron-Asymmetry. 21: 275-276. DOI: 10.1016/J.Tetasy.2010.01.011 |
0.484 |
|
2010 |
Srikrishna A, Sridharan M, Prasad KR. Reaction of dialkyl 2-butynoate with aniline and formaldehyde: revision of the structure of the product Tetrahedron. 66: 3651-3654. DOI: 10.1016/J.Tet.2010.03.084 |
0.643 |
|
2009 |
Prasad KR, Pawar AB. Enantiospecific total synthesis of (+)-lentiginosine Arkivoc. 2010. DOI: 10.3998/Ark.5550190.0011.605 |
0.634 |
|
2009 |
Prasad KR, Gandi VR. Stereoselective Formal Total Synthesis of (-)-Didemniserinolipid B Synlett. 2009: 2593-2596. DOI: 10.1055/S-0029-1217976 |
0.587 |
|
2008 |
Prasad KR, Gholap SL. Stereoselective total synthesis of (+)-cardiobutanolide. The Journal of Organic Chemistry. 73: 2916-9. PMID 18324832 DOI: 10.1021/Jo7025614 |
0.833 |
|
2008 |
Prasad KR, Gholap SL. Stereoselective total synthesis of bioactive styryllactones (+)-goniofufurone, (+)7-epi-goniofufurone, (+)-goniopypyrone, (+)-goniotriol, (+)-altholactone, and (-)-etharvensin. The Journal of Organic Chemistry. 73: 2-11. PMID 17523660 DOI: 10.1021/Jo0702342 |
0.824 |
|
2008 |
Prasad KR, Pawar AB. Facile Enantiospecific Synthesis of Dihydroconduritols E and F Synthesis. 2008: 3155-3159. DOI: 10.1055/S-2008-1067261 |
0.528 |
|
2008 |
Prasad KR, Gandi V. Facile enantiospecific synthesis of (−)-muricatacin Tetrahedron-Asymmetry. 19: 2616-2619. DOI: 10.1016/J.Tetasy.2008.11.004 |
0.605 |
|
2008 |
Prasad KR, Swain B. Corrigendum to "Stereoselective total synthesis of (+)-pinellic acid from L-(+)-tartaric acid" Tetrahedron-Asymmetry. 19: 1636. DOI: 10.1016/J.Tetasy.2008.05.026 |
0.546 |
|
2008 |
Prasad KR, Swain B. Stereoselective total synthesis of (+)-pinellic acid from l-(+)-tartaric acid Tetrahedron-Asymmetry. 19: 1134-1138. DOI: 10.1016/J.Tetasy.2008.04.015 |
0.567 |
|
2007 |
Prasad KR, Chandrakumar A. Stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine [jaspine B]. The Journal of Organic Chemistry. 72: 6312-5. PMID 17625885 DOI: 10.1021/Jo0707838 |
0.608 |
|
2007 |
Prasad KR, Anbarasan P. Enantiodivergent synthesis of both enantiomers of gypsy moth pheromone disparlure. The Journal of Organic Chemistry. 72: 3155-7. PMID 17367199 DOI: 10.1021/Jo070060O |
0.73 |
|
2007 |
Srikrishna A, Satyanarayana G, Prasad KR. RCM-based approach to (±)-cuparene Synthetic Communications. 37: 1511-1516. DOI: 10.1080/00397910701229214 |
0.607 |
|
2007 |
Prasad KR, Dhaware MG. Stereoselective Total Synthesis of Bioactive Styryllactones: 9-Deoxygoniopypyrone, Goniopypyrone and 7-epi-Goniofufurone Synthesis. 2007: 3697-3705. DOI: 10.1055/S-2007-990866 |
0.643 |
|
2007 |
Prasad KR, Dhaware MG. Stereoselective Total Synthesis of (-)-9-Deoxygoniopypyrone Synlett. 2007: 1112-1114. DOI: 10.1055/S-2007-973873 |
0.641 |
|
2007 |
Prasad KR, Gholap SL. Facile stereoselective syntheses of goniodiol, 8-epi-goniodiol and 9-deoxygoniopypyrone Tetrahedron Letters. 48: 4679-4682. DOI: 10.1016/J.Tetlet.2007.05.029 |
0.796 |
|
2007 |
Prasad KR, Penchalaiah K, Choudhary A, Anbarasan P. Stereoselective synthesis of (-)-microcarpalide Tetrahedron Letters. 48: 309-311. DOI: 10.1016/J.Tetlet.2006.11.027 |
0.829 |
|
2007 |
Prasad KR, Anbarasan P. Stereoselective synthesis of (-)-6-acetoxyhexadecanolide: a mosquito oviposition attractant pheromone Tetrahedron Asymmetry. 18: 2479-2483. DOI: 10.1016/J.Tetasy.2007.10.006 |
0.779 |
|
2007 |
Prasad KR, Anbarasan P. Enantioselective synthesis of α-benzyloxy-ω-alkenals: application to the synthesis of (+)-exo-brevicomin, (+)-iso-exo-brevicomin, and (-)-isolaurepan Tetrahedron Asymmetry. 18: 1419-1427. DOI: 10.1016/J.Tetasy.2007.05.014 |
0.779 |
|
2007 |
Prasad KR, Chandrakumar A. Stereoselective syntheses of γ-alkyl (aryl)-α,β-dihydroxy-γ-butyrolactones and naturally occurring lipid guggultetrol Tetrahedron. 63: 1798-1805. DOI: 10.1016/J.Tet.2006.12.037 |
0.514 |
|
2007 |
Prasad KR, Anbarasan P. Stereoselective formal synthesis of (-)-centrolobine Tetrahedron. 63: 1089-1092. DOI: 10.1016/J.Tet.2006.11.062 |
0.759 |
|
2006 |
Prasad KR, Gholap SL. Stereoselective synthesis of (+)-goniothalesdiol. The Journal of Organic Chemistry. 71: 3643-5. PMID 16626158 DOI: 10.1021/Jo060159F |
0.821 |
|
2006 |
Prasad KR, Anbarasan P. An expeditious enantiospecific synthesis of (+)-2-hydroxy-exo-brevicomin Synlett. 2087-2088. DOI: 10.1055/S-2006-948190 |
0.784 |
|
2006 |
Prasad KR, Chandrakumar A. Nucleophilic addition reactions of 1,4-diketones derived from tartaric acid: Synthesis of TADDOL analogues Synthesis. 2159-2166. DOI: 10.1055/S-2006-942422 |
0.587 |
|
2006 |
Prasad KR, Anbarasan P. An enantiospecific synthesis of (+)-hydroxy-exo-brevicomin Tetrahedron Letters. 47: 1433-1435. DOI: 10.1016/J.Tetlet.2005.12.094 |
0.778 |
|
2006 |
Prasad KR, Anbarasan P. Enantiospecific synthesis of (-)-muricatacin from l-(+)-tartaric acid Tetrahedron Asymmetry. 17: 2465-2467. DOI: 10.1016/J.Tetasy.2006.09.017 |
0.742 |
|
2006 |
Prasad KR, Chandrakumar A, Anbarasan P. Asymmetric synthesis of both enantiomers of α-methyl-α-methoxyphenylacetic acid from l-(+)-tartaric acid: formal enantioselective synthesis of insect pheromone (-)-frontalin Tetrahedron Asymmetry. 17: 1979-1984. DOI: 10.1016/J.Tetasy.2006.07.007 |
0.743 |
|
2006 |
Prasad KR, Anbarasan P. Stereoselective synthesis of (+)-boronolide and (-)-5-epi-boronolide Tetrahedron Asymmetry. 17: 1146-1151. DOI: 10.1016/J.Tetasy.2006.03.028 |
0.783 |
|
2006 |
Prasad KR, Anbarasan P. Enantiospecific synthesis of (-)-2-hydroxy-exo-brevicomin Tetrahedron Asymmetry. 17: 850-853. DOI: 10.1016/J.Tetasy.2006.02.023 |
0.771 |
|
2006 |
Prasad KR, Anbarasan P. Enantiodivergent synthesis of both antipodes of hydroxy-exo-brevicomin from l-(+)-tartaric acid Tetrahedron. 62: 8303-8308. DOI: 10.1016/J.Tet.2006.06.053 |
0.73 |
|
2005 |
Davis FA, Nolt MB, Wu Y, Prasad KR, Li D, Yang B, Bowen K, Lee SH, Eardley JH. Asymmetric synthesis of β-amino carbonyl compounds with N-sulfinyl β-amino Weinreb amides Journal of Organic Chemistry. 70: 2184-2190. PMID 15760203 DOI: 10.1021/Jo0402780 |
0.791 |
|
2005 |
Davis FA, Yang B, Deng J, Wu Y, Zhang Y, Rao A, Fang T, Goswami R, Prasad KR, Nolt MB, Anilkumar G. Asymmetric synthesis using sulfinimines (N-sulfinyl imines) Phosphorus, Sulfur and Silicon and the Related Elements. 180: 1109-1117. DOI: 10.1080/10426500590910648 |
0.806 |
|
2005 |
Prasad K, Gholap S. An Expeditious Enantiospecific Total Synthesis of (+)-7-epi-Goniofufurone Synlett. 2005: 3018-3018. DOI: 10.1055/S-2005-921924 |
0.828 |
|
2005 |
Prasad KR, Anbarasan P. Asymmetric synthesis of unsaturated α-benzyloxyaldehydes: An enantioselective synthesis of (+)-exo-brevicomin Tetrahedron Asymmetry. 16: 3951-3953. DOI: 10.1016/J.Tetasy.2005.10.035 |
0.768 |
|
2005 |
Prasad KR, Chandrakumar A. Asymmetric synthesis of α-methoxyarylacetic acid derivatives Tetrahedron Asymmetry. 16: 1897-1900. DOI: 10.1016/J.Tetasy.2005.05.002 |
0.674 |
|
2005 |
Davis FA, Nolt MB, Wu Y, Prasad KR, Li D, Yang B, Bowen K, Lee SH, Eardley JH. Asymmetric Synthesis of β-Amino Carbonyl Compounds with N-Sulfinyl β-Amino Weinreb Amides. Cheminform. 36. DOI: 10.1002/chin.200533085 |
0.724 |
|
2003 |
Davis FA, Prasad KR. Sulfinimine-mediated asymmetric synthesis of β-hydroxy α-amino phosphonates Journal of Organic Chemistry. 68: 7249-7253. PMID 12968873 DOI: 10.1021/Jo0301649 |
0.627 |
|
2003 |
Davis FA, Wu Y, Yan H, McCoull W, Prasad KR. Asymmetric synthesis of aziridine 2-phosphonates from enantiopure sulfinimines (N-sulfinyl imines). Synthesis of α-amino phosphonates Journal of Organic Chemistry. 68: 2410-2419. PMID 12636410 DOI: 10.1021/Jo020707Z |
0.739 |
|
2003 |
Davis FA, Prasad KR, Nolt MB, Wu Y. N-sulfinyl β-amino Weinreb amides: Synthesis of enantiopure β-amino carbonyl compounds. Asymmetric synthesis of (+)-sedridine and (-)-allosedridine Organic Letters. 5: 925-927. PMID 12633107 DOI: 10.1021/Ol034119Z |
0.766 |
|
2002 |
Davis FA, Prasad KR, Carroll PJ. Asymmetric synthesis of polyhydroxy α-amino acids with the sulfinimine-mediated asymmetric Strecker reaction: 2-amino 2-deoxy l-xylono-1,5-lactone (polyoxamic acid lactone) Journal of Organic Chemistry. 67: 7802-7806. PMID 12398506 DOI: 10.1021/Jo020302E |
0.701 |
|
2002 |
Davis FA, Wu Y, Yan H, Prasad KR, McCoull W. 2H-azirine 3-phosphonates: A new class of chiral iminodienophiles. Asymmetric synthesis of quaternary piperidine phosphonates Organic Letters. 4: 655-658. PMID 11843615 DOI: 10.1021/Ol017289P |
0.713 |
|
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