Autoxidation of intermediary mesoionic 1,3-oxazolium-5-olates generated from cyclic N-acyl α-amino acids

DOI: 10.1248/cpb.45.1248

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Chemical and Pharmaceutical Bulletin p. 1248 - 1253 (1997)

Update date:2022-08-05

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Kawase, Masami

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Article abstract of DOI:10.1248/cpb.45.1248

Mesoionic 1,3-oxazolium-5-olates (munchnones) react fairly rapidly with oxygen to give the autoxidation products when the C-4 substituent is aromatic. The autoxidation occurred in the munchnones generated from N-acyl tetrahydroisoquinoline-1-carboxylic ac

Full text of DOI:10.1248/cpb.45.1248

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Article Doi

Autoxidation of intermediary mesoionic 1,3-oxazolium-5-olates generated from cyclic N-acyl α-amino acids

DOI: 10.1248/cpb.45.1248

Source and publish data:

Authors:

Article abstract of DOI:10.1248/cpb.45.1248

Full text of DOI:10.1248/cpb.45.1248

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