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Preparation and Reactions of Pyridinium Ylids via Decarboxylation of Pyridinium Betaines

Preparation and Reactions of Pyridinium Ylids via Decarboxylation of Pyridinium Betaines
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摘要 Pyridinium ylids 4 were generated as reaction intermediates from the decarboxylation of pyridinium betaines 3, which were prepared from the reactions of a-amino acid ester hydrochlorides with 2, 4, 6-triphenylpyrylium tetrafluoroborate. Protonation, addition and substitution reactions of 4 with electrophiles were studied in this paper. Pyridinium ylids 4 were generated as reaction intermediates from the decarboxylation of pyridinium betaines 3, which were prepared from the reactions of a-amino acid ester hydrochlorides with 2, 4, 6-triphenylpyrylium tetrafluoroborate. Protonation, addition and substitution reactions of 4 with electrophiles were studied in this paper.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第7期597-600,共4页 中国化学快报(英文版)
基金 We want to express our sincere appreciation to Professor Joe Wilson of University of Kentucky and Professor Xiulin Ye of Peking University for their favorable suggestions and assistance for the work.
关键词 Pyridinium betaine pyridinium ylid DECARBOXYLATION electrophile. Pyridinium betaine pyridinium ylid decarboxylation electrophile.
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