PRESENTATION OF NEW RESULTS CONCERNIG THE SYNTHESIS OF ENANTIOPURE ORTHOGONALLY PROTECTED EITHER S-(AMINOALKYL) OR Se-(AMINOALKYL) ALPHA-AMINO ACIDS FROM BETA-IODOAMINES AND CYSTEINE OR SELENOCYSTINE RESPECTIVELY IN CONCERT WITH THE PROGRESS IN THE SYNTHESIS OF ENANTIOPURE BETA2,3-AMINO ACIDS FROM n-PROTECTED BETA3-AMINO NITRILES.
Emerging Chemistry from alpha-Amino Acid Homologation Intermediates / Caputo, R., S., C., I., d.P., Longobardo, L.. - STAMPA. - (2006), pp. 65-65. (6th ITALIAN SPANISH SYMPOSIUM ON ORGANIC CHEMISTRY TAORMINA 14-17 LUGLIO 2006).
Emerging Chemistry from alpha-Amino Acid Homologation Intermediates
CAPUTO, ROMUALDO;LONGOBARDO, LUIGI
2006
Abstract
PRESENTATION OF NEW RESULTS CONCERNIG THE SYNTHESIS OF ENANTIOPURE ORTHOGONALLY PROTECTED EITHER S-(AMINOALKYL) OR Se-(AMINOALKYL) ALPHA-AMINO ACIDS FROM BETA-IODOAMINES AND CYSTEINE OR SELENOCYSTINE RESPECTIVELY IN CONCERT WITH THE PROGRESS IN THE SYNTHESIS OF ENANTIOPURE BETA2,3-AMINO ACIDS FROM n-PROTECTED BETA3-AMINO NITRILES.File in questo prodotto:
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