Literature DB >> 12884383

Insect chemistry and chirality.

Patricia Y Hayes1, Mary T Fletcher, Sharon Chow, Matthew J McGrath, Yong Q Tu, Hesheng Zhang, Natasha L Hungerford, Christopher S P McErlean, Jeannette E Stok, Christopher J Moore, James J DeVoss, William Kitching.   

Abstract

Examination of the chemistry of a number of Australian insect species provided examples of unusual structures and encouraged determinations of their absolute stereochemistry by stereocontrolled syntheses and chromatographic comparisons. Inter alia, studies with the fruit-spotting bug (Amblypelta nitida), certain parasitic wasps (Biosteres sp.), the aposematic shield bug (Cantao parentum), and various species of scarab grubs are summarized. The determination of enantiomeric excesses (ee's) for component epoxides, lactones, spiroacetals, and allenes are described. Stereochemical and related aspects of the biosynthesis of spiroacetals in certain fruit-fly species (Bactrocerae sp.) are also presented. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12884383     DOI: 10.1002/chir.10273

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Intrageneric differences in the four stereoisomers of stenusine in the rove beetle genus, Stenus (Coleoptera, Staphylinidae).

Authors:  Inka Lusebrink; Dirk Burkhardt; Thomas Gedig; Konrad Dettner; Armin Mosandl; Karlheinz Seifert
Journal:  Naturwissenschaften       Date:  2006-10-26
  1 in total

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