Simple and highly diastereoselective synthesis of trifluoromethyl-containing myosmines via reaction between 2-(aminomethyl)pyridine and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione-Reference-Cited by-同舟云学术

Simple and highly diastereoselective synthesis of trifluoromethyl-containing myosmines via reaction between 2-(aminomethyl)pyridine and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione

Published:2003-03 Issue:11 Volume:44 Page:2417-2420
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ohkura Hironari,Berbasov Dmitrii O.,A. Soloshonok Vadim

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

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2. A general stereocontrolled synthesis of cis-2,3 disubstituted pyrrolidines and piperidines

3. Organometallic ring-opening reactions of N-acyl and N-alkoxycarbonyl lactams. Synthesis of cyclic imines

4. Stereoselectivity in Reactions of Metal Complexes. Part XI. 2,6-Bis(pyrrolidin-2-yl)pyridine: Synthesis and resolution of themeso and the optically active isomers. Complex formation with copper(II) ion in aqueous solution

5. Eine einfache Synthese von Pyridinalkaloiden

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