regioselective palladium-catalyzed allylic alkylations via anti/syn-π-allyl intermediates
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2004 Aminocarboxylic acids (hydrazinocarboxylic acids) and esters
200430.fm Page 77 Thursday, July 1, 2004 10:50 AM
Aminocarboxylic acids (hydrazinocarboxylic acids) and estersP 0270 Regioselective Palladium-Catalyzed Allylic Alkylations via anti/syn-π-Allyl Inter-
mediates. — The reactive zinc enolate derived from the N-protected glycine ester (I) is used as nucleophile in Pd-catalyzed allylic alkylation reaction. In general, (Z)-allylic substrates give rise to anti/syn-π-allyl Pd-complexes which react regioselectively at the anti-position. — (KAZMAIER*, U.; POHLMAN, M.; Synlett 2004, 4, 623-626; Fachrichtung Org. Chem., Univ. des Saarlandes, D-66041 Saarbruecken, Germany; Eng.) — Mais
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