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Merck

Catalytic asymmetric formation of beta-sultams.

Organic letters (2007-04-24)
Marian Zajac, René Peters
RESUMEN

beta-Sultams, highly strained sulfonyl analogues of beta-lactams, were prepared enantio- and diastereoselectively by tertiary amine catalyzed [2 + 2] cycloaddition reactions. The title compounds are practical precursors of highly enantioenriched biologically interesting beta-aminosulfonyl derivatives.

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Sigma-Aldrich
Sulfuryl chloride, 97%
Sigma-Aldrich
Sulfuryl chloride solution, 1.0 M in methylene chloride
Sigma-Aldrich
3-Chloropropanesulfonyl chloride, 98%