Stereoselective synthesis of β-sultams using chiral tricarbonyl(η6-arene)chromium(0) complexes
✍ Scribed by Clara Baldoli; Paola Del Buttero; Dario Perdicchia; Tullio Pilati
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 471 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
The reaction of (-)lg or (+)-IS-tricarbonyl(2-substituted benzaldehyde)chromium complexes with tertbutylmethanesulfonamide dianion afforded, after decomplexation and intramolecular cyclization, the enantiomerically pure N-tert-butyl-3-(2-phenyl substituted)-1,2-thiazetidine 1,1 dioxide derivatives. The hydrolytic ring opening gave the corresponding enantiopure [3-aminosulfonic acid.
📜 SIMILAR VOLUMES
Oxidation of sulfenyl substituted tricarbonyl(ll6-arene)chrom(o) complexes with Ti(OP& I diethyl lartraw I H20 I cumene hydroperoxide (2:4:2:1.3) gives sulfinyl suhstitured tricarbonyl(q6arcne)chromium(O) complexes in 60.73% yield and 111.86% e.e. (29.60% yield and 90.t95t c e. after cryslallisation