Enantioselective syntheses of Monomorium minutum ant venom alkaloids : (5R)-2-(5-Hexenyl)-5-nonyl-3,4-dihydro-2H-pyrrole and (2R,5R)-2-(5-hexenyl)-5-nonylpyrrolidine from (s)-pyroglutamic acid.-Reference-Cited by-同舟云学术

Enantioselective syntheses of Monomorium minutum ant venom alkaloids : (5R)-2-(5-Hexenyl)-5-nonyl-3,4-dihydro-2H-pyrrole and (2R,5R)-2-(5-hexenyl)-5-nonylpyrrolidine from (s)-pyroglutamic acid.

Published:1991-12 Issue:51 Volume:32 Page:7521-7524
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Rosset S.,Célérier J.P.,Lhommet G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Novel Pyrrolidines in the Venom of the Ant Monomorium indicum

2. Analysis of workerMonomorium minimum ant's venom using gas chromatography/mass spectrometry and gas chromatography/tandem mass spectrometry

3. The α,α′-dialkylation of cyclic amines. The synthesis of ant venoms.

4. Synthesis of (�)-trans-2,5-Dialkylpyrrolidines from theLukes-?orm Dilactam: Efficient Preparation of (�)-trans-2-Butyl-5-heptylpyrrolidine and Analogs Present in Ant Venoms

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