Literature DB >> 17958433

Enantioselective synthesis of the C8-C20 segment of curvicollide C.

Marleen Körner1, Martin Hiersemann.   

Abstract

The enantioselective synthesis of the C8-C20 fragment of curvicollide C has been accomplished. A catalytic asymmetric Claisen rearrangement (CAC), a diastereoselective methyl cupration of an alkynoate, and a Julia-Kocienski olefination served as key C/C-connecting transformations.

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Year:  2007        PMID: 17958433     DOI: 10.1021/ol702092h

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


  6 in total

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Authors:  Annika Gille; Markus Schürmann; Hans Preut; Martin Hiersemann
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-08-30

4.  (3S,4S,5R)-4-Hydr-oxy-3-methyl-5-[(2S,3R)-3-methyl-pent-4-en-2-yl]-4,5-dihydro-furan-2(3H)-one.

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Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-12-17

5.  {2,2-Bis[(4S)-4-isopropyl-4,5-dihydro-1,3-oxazol-2-yl]propane}-bis-(N,N-dimethyl-formamide)-copper(II) bis-[hexa-fluoridoanti-monate(V)].

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Authors:  Ann-Christin Schmidt; Martin Hiersemann
Journal:  Chemistry       Date:  2021-12-09       Impact factor: 5.020

  6 in total

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