Literature DB >> 10788580

The use of polymer-bound triphenylphosphine in the stereochemical inversion of secondary alcohols.

J M White1, A R Tunoori, D Dutta, G I Georg.   

Abstract

Polymer-bound triphenylphosphine can replace triphenylphosphine in the Mitsunobu reaction to generate stereochemically inverted secondary alcohols. This method is comparable with the standard Mitsunobu reaction in terms of inversion of stereochemistry, yield, and reaction time, even for sterically very hindered secondary alcohols. The special merit of this reaction is that the excess polymer-bound triphenylphosphine and its by-products are easily removed by filtration from the reaction products.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10788580     DOI: 10.2174/1386207003331706

Source DB:  PubMed          Journal:  Comb Chem High Throughput Screen        ISSN: 1386-2073            Impact factor:   1.339


  2 in total

1.  C4-alkylthiols with activity against Moraxella catarrhalis and Mycobacterium tuberculosis.

Authors:  Maya B Kostova; Carey J Myers; Tim N Beck; Balbina J Plotkin; Jacalyn M Green; Helena I M Boshoff; Clifton E Barry; Jeffrey R Deschamps; Monika I Konaklieva
Journal:  Bioorg Med Chem       Date:  2011-10-01       Impact factor: 3.641

Review 2.  Polymer-supported triphenylphosphine: application in organic synthesis and organometallic reactions.

Authors:  Ziad Moussa; Zaher M A Judeh; Saleh A Ahmed
Journal:  RSC Adv       Date:  2019-11-05       Impact factor: 4.036

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.