Literature DB >> 21671632

Asymmetric synthesis of chiral δ-lactones containing multiple contiguous stereocenters.

Jennifer Peed1, Ignacio Periñán Domínguez, Iwan R Davies, Matt Cheeseman, James E Taylor, Gabriele Kociok-Köhn, Steven D Bull.   

Abstract

A versatile methodology for the asymmetric synthesis of chiral δ-lactones containing multiple contiguous stereocenters has been developed that relies on a series of Evans' aldol, hydroxyl-directed cyclopropanation, methanolysis, and Hg(II) mediated cyclopropane ring-opening reactions for stereocontrol.
© 2011 American Chemical Society

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Year:  2011        PMID: 21671632     DOI: 10.1021/ol2012023

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


  1 in total

1.  Solid-phase asymmetric synthesis using a polymer-supported chiral Evans'-type oxazolidin-2-one.

Authors:  Rachel Green; Jennifer Peed; James E Taylor; Richard A R Blackburn; Steven D Bull
Journal:  Nat Protoc       Date:  2013-09-12       Impact factor: 13.491

  1 in total

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