Unusual stereochemical outcome of radical cyclization: synthesis of (+)-biotin
Title | Unusual stereochemical outcome of radical cyclization: synthesis of (+)-biotin |
Publication Type | Journal Article |
Year of Publication | 2005 |
Authors | Chavan, SP, Chittiboyina, AG, Ramakrishna, G, Tejwani, RB, Ravindranathan, T, Kamat, SK, Rai, B, Sivadasan, L, Balakrishnan, K, Ramalingam, S, Deshpande, VH |
Journal | Tetrahedron |
Volume | 61 |
Issue | 39 |
Pagination | 9273-9280 |
Date Published | SEP |
Type of Article | Article |
ISSN | 0040-4020 |
Keywords | biotin, exocyclization, radical cyclization |
Abstract | An enantioselective synthesis of (+)-biotin 1 starting from naturally available cysteine is described. The key steps are the unusual stereochemical outcome of radical cyclization of compound 10 to prepare 5,5-fused system 11, and the introduction of C4-sidechain at C-6 in 13 via a Grignard reaction. (c) 2005 Elsevier Ltd. All rights reserved. |
DOI | 10.1016/j.tet.2005.07.070 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.645 |
Divison category:
Organic Chemistry