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STEREOSELECTIVE SYNTHESIS OF UNSATURATED POLYHYDROXYLATED AMINO-ACIDSVIA ESTER ENOLATE CLAISEN REARRANGEMENT

Authors

KAZMAIER U SCHNEIDER C

Citation

U. Kazmaier et C. Schneider, STEREOSELECTIVE SYNTHESIS OF UNSATURATED POLYHYDROXYLATED AMINO-ACIDSVIA ESTER ENOLATE CLAISEN REARRANGEMENT, Synlett, (10), 1996, pp. 975

Citations number

Categorie Soggetti

Chemistry Inorganic & Nuclear

Journal title

Synlett → ACNP

ISSN journal

09365214

Issue

Year of publication

1996

Database

ISI

SICI code

0936-5214(1996):10<975:SSOUPA>2.0.ZU;2-N

Abstract

Ester enolate Claisen rearrangement of chelated N-protected chiral all ylic amino acid esters results in the formation of polyhydroxylated ga mma,delta-unsaturated amino acids in good yields and with a high degre e of chirality transfer.