Asymmetric synthesis of (1R,8S)- and (1S,8S)-1-hydroxypyrrolizidin-3-ones via the aldol reaction between N-boc-(S)-prolinal and chiral acetate enolate equivalents derived from (S)- and (R)-[(η5-C5H5)Fe(CO)(PPh3)COCH3]-Reference-Cited by-同舟云学术

Asymmetric synthesis of (1R,8S)- and (1S,8S)-1-hydroxypyrrolizidin-3-ones via the aldol reaction between N-boc-(S)-prolinal and chiral acetate enolate equivalents derived from (S)- and (R)-[(η5-C5H5)Fe(CO)(PPh3)COCH3]

Published:1992-01 Issue:1 Volume:3 Page:123-136
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Beckett R. Paul,Davies Stephen G.,Mortlock Andrew A.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference19 articles.

1. Synthesis of pyrrolizidine alkaloids indicine, intermedine, lycopsamine, and analogs and their N-oxides. Potential antitumor agents

2. Enantioselective synthesis of seven pyrrolizidine diols from a single precursor

3. Synthetic studies on pyrrolizidine alkaloid antitumor agents. Enantioselective synthesis of retronecine and its enantiomer from D-glucose

4. Free radical cyclizations in alkaloid synthesis: (+)-heliotridine and (+)-hastanecine

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