Diastereoselective Amidoalkylation of (3S,7aR)-6-Benzyl-7-hydroxy-3-phenyltetra- hydro-5H-imidazo[1,5-c][1,3]thiazol-5-one : A Short and Highly Efficient Synthesis of (+)-Biotin-Reference-Cited by-同舟云学术

Diastereoselective Amidoalkylation of (3S,7aR)-6-Benzyl-7-hydroxy-3-phenyltetra- hydro-5H-imidazo[1,5-c][1,3]thiazol-5-one : A Short and Highly Efficient Synthesis of (+)-Biotin

Published:2005-01-27 Issue:5 Volume:70 Page:1901-1903
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chavan Subhash P.¹,Chittiboyina Amar G.¹,Ravindranathan T.¹,Kamat Subhash K.¹,Kalkote Uttam R.¹

Affiliation:

1. Division of Organic Chemistry: Technology, National Chemical Laboratory, Pune, India 411 008 spchavan@dalton.ncl.res.in

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0488107

Reference18 articles.

1. Biotin: A Timeless Challenge for Total Synthesis

2. 2-Thiazolidinone: a novel thiol protective surrogate of complete atom efficiency, a practical synthesis of (+)-biotin

3. A Switch of Reactivity Profile in Ionic Intramolecular Annulation Reactions: A Short and Efficient Synthesis of d-(+)-Biotin

4. Total synthesis of d-(+)-biotin

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