Synthesis of (R)- 3-alkyl-3-benzyl-2-azetidinones in enantiomerically pure form

DOI: 10.1016/S0957-4166(00)82343-5

Source and publish data:

Tetrahedron Asymmetry p. 229 - 238 (1993)

Update date:2022-08-04

Topics:

Authors:

Cativiela

Diaz-de-Villegas

Galvez Galvez

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Article abstract of DOI:10.1016/S0957-4166(00)82343-5

The diastereoselective alkylation of the enolate of 10-dicyclohexylsulfamoylisobornyl 3-phenyl-2-cyanopropanoate is reported. This alkylation took place with very good yield and selectivity and the reaction product was reduced and cyclised to the correspo

Full text of DOI:10.1016/S0957-4166(00)82343-5

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Product name:(2RS)-(1S,2R,4R)-10-(Dicyclohexylsulfamoyl)isobornyl 3-phenyl-2-cyanopropanoate

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