Co(III)-salen catalyzed carbenoid reaction: Stereoselective [2,3]sigmatropic rearrangement of S-ylides derived from allyl aryl sulfides
โ Scribed by Tsutomu Fukuda; Tsutomu Katsuki
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 224 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Allyi aryl sulfides and diazoacetic acid esters react in the presence of optically active Co(lll)salen complex (4) with good enantioselectivity, to give the [2,31sigmatropic rearrangement products, 2arylthio-3-aryl-4-pentenoic acid esters, via the corresponding S-ylides.
๐ SIMILAR VOLUMES
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