Literature DB >> 22900915

A chiron approach to aminocytitols by Petasis-Borono-Mannich reaction: formal synthesis of (+)-conduramine E and (-)-conduramine E.

Partha Ghosal1, Arun K Shaw.   

Abstract

A chiron approach to a stereoselective route for the synthesis of aminocytitols from carbohydrates is described. The formal synthesis of (+)-conduramine E and (-)-conduramine E was achieved by utilizing this strategy. The key features of the synthetic strategy include one-pot three-component Petasis-Borono-Mannich reaction to introduce the syn-β-amino alcohol functionality of conduramine E and ring-closing metathesis to construct its carbocyclic core. The present synthetic approach paves the way for stereoselective synthesis of several conduramines starting from carbohydrates.

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Year:  2012        PMID: 22900915     DOI: 10.1021/jo300804d

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Diastereo- and regioselective petasis aryl and allyl boration of ninhydrins towards synthesis of functionalized indene-diones and dihydrobenzoindeno-oxazin-ones.

Authors:  Ayon Sengupta; Suvendu Maity; Pinaki Saha; Prasanta Ghosh; Sonali Rudra; Chhanda Mukhopadhyay
Journal:  Mol Divers       Date:  2022-08-01       Impact factor: 3.364

2.  Reactivity and Synthetic Applications of Multicomponent Petasis Reactions.

Authors:  Peng Wu; Michael Givskov; Thomas E Nielsen
Journal:  Chem Rev       Date:  2019-08-27       Impact factor: 60.622

  2 in total

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