PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched beta -amino-alpha -substituted phosphonic acids.
Camphor-based chiral auxiliary: Formal synthesis of enantiomerically enriched beta-aminophosphonic acids via PTC alkylation / G. Cravotto, G. Giovenzana, R. Pagliarin, G. Palmisano, M. Sisti. - In: SYNTHETIC COMMUNICATIONS. - ISSN 0039-7911. - 31:7(2001), pp. 1013-1020. [10.1081/SCC-100103530]
Camphor-based chiral auxiliary: Formal synthesis of enantiomerically enriched beta-aminophosphonic acids via PTC alkylation
R. Pagliarin;
2001
Abstract
PTC-alkylation of a chiral non-racemic cyanomethyl phosphonic acid equivalent embodying the camphor skeleton gave rise to a formal entry into enantiomerically enriched beta -amino-alpha -substituted phosphonic acids.
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