Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vinay Shankar, Tiwari"'
Autor:
Vinay Shankar Tiwari, Prince Joshi, Kanchan Yadav, Anamika Sharma, Sushobhan Chowdhury, Ashan Manhas, Niti Kumar, Renu Tripathi, Wahajul Haq
Publikováno v:
ACS Omega, Vol 6, Iss 20, Pp 12984-12994 (2021)
Externí odkaz:
https://doaj.org/article/4b06e4d5f42645c7acffd8bec9ae993a
Autor:
Izhar Ron, Ie Mei Bhattacharyya, Vinay Shankar Tiwari, Doron Greental, Ruth Shima-Edelstein, Evgeny Pikhay, Yakov Roizin, Barak Akabayov, Gil Shalev
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57a13c96ec57c70e26a1cca9555d320d
https://doi.org/10.2139/ssrn.4290996
https://doi.org/10.2139/ssrn.4290996
Autor:
Anamika Sharma, Ashan Manhas, Renu Tripathi, Prince Joshi, Vinay Shankar Tiwari, Wahajul Haq, Sushobhan Chowdhury, Niti Kumar, Kanchan Yadav
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 20, Pp 12984-12994 (2021)
ACS Omega, Vol 6, Iss 20, Pp 12984-12994 (2021)
A series of novel 4-aminoquinoline analogues bearing a methyl group at 4-aminoquinoline moiety were synthesized via a new and robust synthetic route comprising in situ tert-butoxycarbonyl (Boc) deprotection-methylation cascade resulting in the corres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc54012a2da140ef04909ff1f86701f
https://pubmed.ncbi.nlm.nih.gov/34056449
https://pubmed.ncbi.nlm.nih.gov/34056449
Publikováno v:
Organic & Biomolecular Chemistry. 17:4460-4464
An expeditious method for the synthesis of homo and heterochiral dipeptides containing l-alanine and d/l 2-methyl allo-hydroxyl prolines was developed using direct aminolysis of bicyclic lactones derived from d/l alanine. The impact of C-2 methylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86416a2eaecd54c53ca722f3799e6e6e
https://doi.org/10.1039/c9ob00150f
https://doi.org/10.1039/c9ob00150f
Publikováno v:
Tetrahedron: Asymmetry. 27:865-871
4-Hydroxy-2-methylproline diastereomers are successfully prepared without the use of an external chiral auxiliary. Dihydroxylation of the key intermediate 2 resulted in lactone 4 as a mixture of diastereomers in good yield. Mesylation, hydrogenation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97d18c77b6cc2259cbb5f414cdbc8726
https://doi.org/10.1016/j.tetasy.2016.07.001
https://doi.org/10.1016/j.tetasy.2016.07.001
Publikováno v:
Chirality. 27:619-624
A simple and stereoselective synthesis of 3-methylthalidomide, a configurationally stable thalidomide analog, is presented. Herein we describe the synthesis of (R)-3-methylthalidomide starting from (S)-alanine by piperidin-2-one ring assembly approac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d1fc4b21ae7ec518f9125bba5dfd967
https://doi.org/10.1002/chir.22474
https://doi.org/10.1002/chir.22474
Publikováno v:
Chirality. 27(9)
A simple and stereoselective synthesis of 3-methylthalidomide, a configurationally stable thalidomide analog, is presented. Herein we describe the synthesis of (R)-3-methylthalidomide starting from (S)-alanine by piperidin-2-one ring assembly approac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::574851fade1cf91095130425a4754fe8
https://pubmed.ncbi.nlm.nih.gov/26079113
https://pubmed.ncbi.nlm.nih.gov/26079113