Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ravindra S. Topgi"'
Publikováno v:
ChemInform. 23
6,6′-Diamino-2,2′-bipyridine was synthesized in moderate yield by a dependable four step procedure.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757813d63abc95828732c71e6bef4457
https://doi.org/10.1002/chin.199235197
https://doi.org/10.1002/chin.199235197
Publikováno v:
Synthetic Communications. 22:1033-1037
6,6′-Diamino-2,2′-bipyridine was synthesized in moderate yield by a dependable four step procedure.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49de0b6de83d003860520a3782bc9b8b
https://doi.org/10.1080/00397919208019294
https://doi.org/10.1080/00397919208019294
Autor:
Ravindra S. Topgi
Publikováno v:
Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::513d3b25a7570c44b3679b97cb72478e
https://doi.org/10.1002/3527602151.ch25
https://doi.org/10.1002/3527602151.ch25
Autor:
Ravindra S. Topgi
Publikováno v:
ACS Symposium Series ISBN: 9780841236790
Applied Biocatalysis in Specialty Chemicals and Pharmaceuticals
Applied Biocatalysis in Specialty Chemicals and Pharmaceuticals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fedb9883c3f364af7ec01174bb3765c1
https://doi.org/10.1021/bk-2001-0776.ch014
https://doi.org/10.1021/bk-2001-0776.ch014
Publikováno v:
Bioorganicmedicinal chemistry. 7(10)
The beta-amino acid, (S)-ethyl-3-amino-4-pentynoate, is a chiral synthon used in the synthesis of xemilofiban hydrochloride, an anti-platelet agent. A biocatalytic approach was developed to resolve (R)- and (S)-enantiomers of ethyl 3-amino-4-pentynoa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8820908316acb480a43e96d25d00288
https://pubmed.ncbi.nlm.nih.gov/10579530
https://pubmed.ncbi.nlm.nih.gov/10579530
Publikováno v:
The Journal of biological chemistry. 271(1)
Bacterial luciferase catalyzes the emission of visible light from the reaction of reduced flavin, molecular oxygen, and an n-alkyl aldehyde. The mechanism of the reaction was probed by measuring the electronic effects of various substituents at the 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::801953fb3f97576b68793e8ca2dacdf3
https://pubmed.ncbi.nlm.nih.gov/8550543
https://pubmed.ncbi.nlm.nih.gov/8550543
Autor:
BADAL C. SAHA, DAVID C. DEMIRJIAN, S. L. Neidleman, Francisco Moris-Varas, Laura Hartman, Amit Shah, T. M. Kuo, T. Kaneshiro, Paul P. Taylor, Nigel J. Grinter, Shelly L. McCarthy, David P. Pantaleone, Jennifer L. Ton, Roberta K. Yoshida, Ian G. Fotheringham, Kiyoshi Hayashi, Qin Wang, Satoru Nirasawa, Tsuyoshi Simonishi, Motomitsu Kitaoka, Satoshi Kaneko, Ching T. Hou, Hugh O'Neill, Jonathan Woodward, Shang-Tian Yang, Julia A. Bednarcik, A. F. Hsu, T. A. Foglia, K. Jones, S. Shen, Tamara D. Dukes, Kurt R. Vogler, Daniel R. Beacom, Bruce E. Meincke, L. Kirk Behrendt, Richard F. Senkpeil, Weiguo Liu, J. David Rozzell, Ravindra S. Topgi, Ramesh N. Patel, Ronald L. Hanson, Jong-Shik Shin, Byung-Gee Kim, Per Berglund, Maria Christiernin, Erik Hedenström