Literature DB >> 15876042

A modular approach to polyketide building blocks: cycloadditions of nitrile oxides and homoallylic alcohols.

Nina Lohse-Fraefel1, Erick M Carreira.   

Abstract

A general approach to the diastereoselective synthesis of Delta(2)-isoxazolines via magnesium-mediated, hydroxyl-directed diastereoselective nitrile oxide cycloadditions of homoallylic alcohols and monoprotected homoallylic diols is disclosed. A broad spectrum of aliphatic and aromatic nitrile oxides and a variety of homoallylic alcohols participate in the cycloaddition, thus expanding the scope of polyketide building blocks that can be accessed using this strategy.

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Year:  2005        PMID: 15876042     DOI: 10.1021/ol0504953

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


  2 in total

1.  Transition structures of diastereoselective 1,3-dipolar cycloadditions of nitrile oxides to chiral homoallylic alcohols.

Authors:  Jennifer A R Luft; Kieche Meleson; K N Houk
Journal:  Org Lett       Date:  2007-01-25       Impact factor: 6.005

2.  Novel approach to multifunctionalized homoallylic alcohols via regioselective ring opening of aryl oxiranes with 3-iodo allenoates.

Authors:  Adiseshu Kattuboina; Parminder Kaur; Cody Timmons; Guigen Li
Journal:  Org Lett       Date:  2006-06-22       Impact factor: 6.005

  2 in total

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