New versatile approach to α-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction

V. Atlan; L. El Kaim; C. Supiot

doi:10.1039/b003361h

New versatile approach to α-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction

V. Atlan
, L. El Kaim
, C. Supiot

Unité Chimie et Procédés

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

Abstract

Addition of diazonium tetrafluoroborates to an acyl chloride pyridine mixture affords hydrazonoacid derivatives in smooth conditions; this new Japp-Klingemann reaction emphasizes the synthetic potential of electrophilic addition to ketenes.

Original language	English
Pages (from-to)	1385-1386
Number of pages	2
Journal	Chemical Communications
Issue number	15
DOIs	https://doi.org/10.1039/b003361h
Publication status	Published - 7 Aug 2000
Externally published	Yes

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title = "New versatile approach to α-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction",

abstract = "Addition of diazonium tetrafluoroborates to an acyl chloride pyridine mixture affords hydrazonoacid derivatives in smooth conditions; this new Japp-Klingemann reaction emphasizes the synthetic potential of electrophilic addition to ketenes.",

author = "V. Atlan and \{El Kaim\}, L. and C. Supiot",

year = "2000",

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doi = "10.1039/b003361h",

language = "English",

pages = "1385--1386",

journal = "Chemical Communications",

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T1 - New versatile approach to α-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction

AU - Atlan, V.

AU - El Kaim, L.

AU - Supiot, C.

PY - 2000/8/7

Y1 - 2000/8/7

N2 - Addition of diazonium tetrafluoroborates to an acyl chloride pyridine mixture affords hydrazonoacid derivatives in smooth conditions; this new Japp-Klingemann reaction emphasizes the synthetic potential of electrophilic addition to ketenes.

AB - Addition of diazonium tetrafluoroborates to an acyl chloride pyridine mixture affords hydrazonoacid derivatives in smooth conditions; this new Japp-Klingemann reaction emphasizes the synthetic potential of electrophilic addition to ketenes.

U2 - 10.1039/b003361h

DO - 10.1039/b003361h

M3 - Article

AN - SCOPUS:0034617856

SN - 1359-7345

SP - 1385

EP - 1386

JO - Chemical Communications

JF - Chemical Communications

IS - 15

ER -

New versatile approach to α-hydrazonoesters and amino acid derivatives through a modified Japp-Klingemann reaction

Abstract

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