Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from carbenoids and propargyl sulfides
โ Scribed by Xiaomei Zhang; Ming Ma; Jianbo Wang
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 203 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0957-4166
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โฆ Synopsis
Catalytic asymmetric [2,3] sigmatropic rearrangement of sulfur ylides generated from aryldiazoacetates and propargyl sulfides with a number of chiral Rh(II) and Cu(I) catalysts have been investigated and moderately high enantioselectivities (up to 81% ee) have been achieved.
๐ SIMILAR VOLUMES
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Reaction of allyl aryl sulfides and a-diazoacetic acid esters in the presence of optically active Co(HD-salen complex (8-Br) provided 3-substituted 2-arylthio-4-pentenoic acid esters stereo~l~vely by way of enantioselcctive S-ylide formation and subse~luent diastereoselective [2,3]sismalropic rearra