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Electrospray ionization mass spectrometric studies of nucleophilic carbenes derived from pyrazolium and indazolium carboxylates.

作者信息

Schmidt Andreas, Habeck Tobias, Merkel Lars, Mäkinen Marko, Vainiotalo Pirjo

机构信息

Clausthal University of Technology, Institute of Organic Chemistry, Leibnizstrasse 6, D-38678 Clausthal-Zellerfeld, Germany.

出版信息

Rapid Commun Mass Spectrom. 2005;19(16):2211-6. doi: 10.1002/rcm.2048.

DOI:10.1002/rcm.2048
PMID:16015672
Abstract

Pyrazolium-3-carboxylate and indazolium-3-carboxylate, which belong to the class of pseudo-cross-conjugated mesomeric betaines and which represent the electronically relevant partial structures of the betaine alkaloid Nigellicin, were examined by electrospray ionization mass spectrometry. These compounds decarboxylate to pyrazol-3-ylidene and indazol-3-ylidene. The formation of adducts of these new nucleophilic carbenes under the measurement conditions was examined.

摘要

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