Literature DB >> 12404500

First Desymmetrization of a Centrosymmetric Molecule in Natural Product Synthesis: Preparation of a Key Fragment in the Synthesis of Hemibrevetoxin B This work was supported by the University of Leeds (through a Brotherton Scholarship to J.M.H.) and Pfizer. We are extremely grateful to Professor T. Nakata of the Institute of Physical and Chemical Research (RIKEN), Saitama, Japan, for providing us with the NMR spectra of the epoxide 2, the Royal Society for a grant, and AstraZeneca for strategic research funding.

Joanne M. Holland1, Mark Lewis, Adam Nelson.   

Abstract

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Year:  2001        PMID: 12404500

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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  2 in total

1.  18O assisted analysis of a γ,δ-epoxyketone cyclization: synthesis of the C16-C28 fragment of ammocidin D.

Authors:  Stephen T Chau; Yoichi Hayakawa; Gary A Sulikowski
Journal:  Org Lett       Date:  2011-01-19       Impact factor: 6.005

2.  Inspirations, discoveries, and future perspectives in total synthesis.

Authors:  K C Nicolaou
Journal:  J Org Chem       Date:  2009-02-06       Impact factor: 4.354

  2 in total

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