ChemInform Abstract: Highly Stereoselective Iodolactonization of 4,5-Allenoic Acids - An Efficient Synthesis of 5-(1′-Iodo-1′(Z)-alkenyl)-4,5-dihydro-2(3H)-furanones

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Bibliographic Details
Published inChemInform Vol. 40; no. 8; p. no
Main Authors Jiang, Xinpeng, Fu, Chunling, Ma, Shengming
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 24.02.2009
WILEY‐VCH Verlag
Subjects
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
e/z-selectivity (incl. e/z-isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
furan derivatives
halogenation
ring closure reactions
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Summary:ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Bibliography:istex:9DD9B2155F4932D2C38D50372E1FD224057B6CF7
ark:/67375/WNG-PPC9K4CL-S
ArticleID:CHIN200908132
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.200908132