A new pyridine synthesis from azoenamines

Didier Coffinier; Laurent El Kaim; Laurence Grimaud; Simon Hadrot

doi:10.1016/j.tetlet.2010.09.098

A new pyridine synthesis from azoenamines

Didier Coffinier
, Laurent El Kaim
, Laurence Grimaud
, Simon Hadrot

Laboratoire de Synthèse Organique

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

Abstract

Azoenamines are formed during the interaction of α-ketohydrazones with secondary amines. These compounds can be converted into pyridines when treated with acetylenedicarboxylates under basic conditions.

Original language	English
Pages (from-to)	6186-6188
Number of pages	3
Journal	Tetrahedron Letters
Volume	51
Issue number	47
DOIs	https://doi.org/10.1016/j.tetlet.2010.09.098
Publication status	Published - 24 Nov 2010
Externally published	Yes

Keywords

Azoenamine
Enamine
Hydrazones
Pyridines

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10.1016/j.tetlet.2010.09.098

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@article{67d306fdfce5476fbe3a6c364ae8f880,

title = "A new pyridine synthesis from azoenamines",

abstract = "Azoenamines are formed during the interaction of α-ketohydrazones with secondary amines. These compounds can be converted into pyridines when treated with acetylenedicarboxylates under basic conditions.",

keywords = "Azoenamine, Enamine, Hydrazones, Pyridines",

author = "Didier Coffinier and \{El Kaim\}, Laurent and Laurence Grimaud and Simon Hadrot",

year = "2010",

month = nov,

day = "24",

doi = "10.1016/j.tetlet.2010.09.098",

language = "English",

volume = "51",

pages = "6186--6188",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - A new pyridine synthesis from azoenamines

AU - Coffinier, Didier

AU - El Kaim, Laurent

AU - Grimaud, Laurence

AU - Hadrot, Simon

PY - 2010/11/24

Y1 - 2010/11/24

N2 - Azoenamines are formed during the interaction of α-ketohydrazones with secondary amines. These compounds can be converted into pyridines when treated with acetylenedicarboxylates under basic conditions.

AB - Azoenamines are formed during the interaction of α-ketohydrazones with secondary amines. These compounds can be converted into pyridines when treated with acetylenedicarboxylates under basic conditions.

KW - Azoenamine

KW - Enamine

KW - Hydrazones

KW - Pyridines

U2 - 10.1016/j.tetlet.2010.09.098

DO - 10.1016/j.tetlet.2010.09.098

M3 - Article

AN - SCOPUS:77958511328

SN - 0040-4039

VL - 51

SP - 6186

EP - 6188

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 47

ER -

A new pyridine synthesis from azoenamines

Abstract

Keywords

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