Abstract
Trifluoroacetic acid- and fluoride anion-promoted 1,3-cycloadditions of N-benzyl-N-(methoxymethyl)trimethylsilylmethylamine to dipolarophiles were found to proceed via the ambivalent azomethine ylide intermediates. © 1985, The Pharmaceutical Society of Japan. All rights reserved.
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Terao, Y., Kotaki, H., Imai, N., & Achiwa, K. (1985). A definite evidence on the ambivalent azomethine ylide intermediate in trifluoroacetic acid- and fluoride anion-promoted 1,3-cyclo-additions involving the silicon-carbon bond cleavage. Chemical and Pharmaceutical Bulletin, 33(2), 896–898. https://doi.org/10.1248/cpb.33.896
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