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

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

18 Citations (Scopus)

Résumé

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.

langue originale	Anglais
Pages (de - à)	1385-1386
Nombre de pages	2
journal	Chemical Communications
Numéro de publication	15
Les DOIs	https://doi.org/10.1039/b003361h
état	Publié - 7 août 2000
Modification externe	Oui

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10.1039/b003361h

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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",

month = aug,

day = "7",

doi = "10.1039/b003361h",

language = "English",

pages = "1385--1386",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "15",

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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

Résumé

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