Chiral sulfoxide controlled asymmetric additions to C-N double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds

DOI: 10.1016/S0040-4020(98)00779-0

Source and publish data:

Tetrahedron p. 12789 - 12806 (1998)

Update date:2022-08-02

Topics:

Authors:

Bravo, Pierfrancesco

Guidetti, Maurizia

Viani, Fiorenza

Zanda, Matteo

Markovsky, Andrey L.

Sorochinsky, Alexander E.

Soloshonok, Irina V.

Soloshonok, Vadim A.

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Article abstract of DOI:10.1016/S0040-4020(98)00779-0

This paper presents a full account of studies into the asymmetric addition reactions between α-lithium derivatives of enantiomerically pure methyl and benzyl p-tolyl sulfoxides and the N-(p-methoxyphenyl)aldimines, bearing trifluoromethyl, pentafluoroethy

Full text of DOI:10.1016/S0040-4020(98)00779-0

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