Literature DB >> 12605494

Enantioselective syntheses of ring-C precursors of vit. B(12). Reagent control.

Peter A Jacobi1, Yongkai Li.   

Abstract

Enelactones of the general structure S-(-)-I were prepared in three steps from alcohol 21 and acids 22 (ee approximately 85%). Lactones S-(-)-I are versatile precursors to enelactams II of the type found in Vitamin B(12).

Entities:  

Mesh：

Substances：

Year:  2003        PMID： 12605494     DOI： 10.1021/ol0275116

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Design, synthesis, and biological evaluation of EF- and ABEF- analogues of (+)-spongistatin 1.

Authors:  Amos B Smith; Christina A Risatti; Onur Atasoylu; Clay S Bennett; Karen Tendyke; Qunli Xu
Journal:  Org Lett       Date:  2010-04-16       Impact factor: 6.005

2.  Scalable Regioselective and Stereoselective Synthesis of Functionalized (E)-4-Iodobut-3-en-1-ols: Gram-Scale Total Synthesis of Fungal Decanolides and Derivatives.

Authors:  Alexander M Sherwood; Samuel E Williamson; Stephanie N Johnson; Anil Yilmaz; Victor W Day; Thomas E Prisinzano
Journal:  J Org Chem       Date:  2018-01-08       Impact factor: 4.354

3.  Design, synthesis, and biological evaluation of diminutive forms of (+)-spongistatin 1: lessons learned.

Authors:  Amos B Smith; Christina A Risatti; Onur Atasoylu; Clay S Bennett; Junke Liu; Hongsheng Cheng; Karen TenDyke; Qunli Xu
Journal:  J Am Chem Soc       Date:  2011-08-12       Impact factor: 15.419
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.