Volume 31, Issue 7
Natural Products
Full Access

ChemInform Abstract: Enantioselective Highly Efficient Synthesis of (-)-Cephalotaxine Using Two Palladium-Catalyzed Transformations.

Lutz F. Tietze

Lutz F. Tietze

Inst. Org. Chem., Georg-August-Univ., D-37077 Goettingen, Germany

Search for more papers by this author
Hartmut Schirok

Hartmut Schirok

Inst. Org. Chem., Georg-August-Univ., D-37077 Goettingen, Germany

Search for more papers by this author
First published: 10 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The highly efficient synthesis of title compound (I) involves enantioselective reduction of the brominated cyclopentenone derivative (II) for introduction of chirality and two successive Pd-catalyzed reactions as key reactions, i.e. allylation of sec. amine (V) with complete retention and diastereoselective Heck reaction of spirocyclic amine (VI).

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.