Stereospecific diaza-Cope rearrangement as an efficient tool for the synthesis of DPEDA pyridine analogs and related C2-symmetric organocatalysts-Reference-Cited by-同舟云学术

Stereospecific diaza-Cope rearrangement as an efficient tool for the synthesis of DPEDA pyridine analogs and related C2-symmetric organocatalysts

Published:2017 Issue:33 Volume:15 Page:7028-7033
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kucherenko A. S.¹²³⁴,Kostenko A. A.¹²³⁴,Gerasimchuk V. V.¹²³⁴,Zlotin S. G.¹²³⁴^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry

2. Russian Academy of Sciences

3. Moscow

4. Russia

Abstract

Enantiomerically pure trans-1,2-di-(pyridinyl)ethylene-1,2-diamines were synthesized via a stereospecific diaza-Cope rearrangement and converted to prolinamide-based recyclable organocatalysts.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01852E

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