Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides

Yasuhiro Maeda; Naohiro Shirai; Yoshiro Sato

doi:10.1039/p19940000393

Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides

Yasuhiro Maeda, Naohiro Shirai, Yoshiro Sato

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12 Citations (Scopus)

Abstract

N,N-Dimethyl(pyridylmethyl)ammonium N-methylides 2, 6, 11, N,N-dimethyl(1-methylpyrrolyl-methyl)ammonium N-methylides 15, 20 and N,N-dimethyl(1-methylindolylmethyl)ammonium N-methylides 23, 28 were generated by fluoride ion-induced desilylation of the corresponding (trimethylsilyl) methylammonium salts 1,5,10,14,19,22 and 27, and the isomerization products of the ylides were investigated.

Original language	English
Pages (from-to)	393-398
Number of pages	6
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	4
DOIs	https://doi.org/10.1039/p19940000393
Publication status	Published - 1994
Externally published	Yes

All Science Journal Classification (ASJC) codes

General Chemistry

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Maeda, Y., Shirai, N., & Sato, Y. (1994). Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides. Journal of the Chemical Society, Perkin Transactions 1, (4), 393-398. https://doi.org/10.1039/p19940000393

Maeda, Yasuhiro ; Shirai, Naohiro ; Sato, Yoshiro. / Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides. In: Journal of the Chemical Society, Perkin Transactions 1. 1994 ; No. 4. pp. 393-398.

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title = "Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides",

abstract = "N,N-Dimethyl(pyridylmethyl)ammonium N-methylides 2, 6, 11, N,N-dimethyl(1-methylpyrrolyl-methyl)ammonium N-methylides 15, 20 and N,N-dimethyl(1-methylindolylmethyl)ammonium N-methylides 23, 28 were generated by fluoride ion-induced desilylation of the corresponding (trimethylsilyl) methylammonium salts 1,5,10,14,19,22 and 27, and the isomerization products of the ylides were investigated.",

author = "Yasuhiro Maeda and Naohiro Shirai and Yoshiro Sato",

year = "1994",

doi = "10.1039/p19940000393",

language = "English",

pages = "393--398",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

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Maeda, Y, Shirai, N & Sato, Y 1994, 'Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides', Journal of the Chemical Society, Perkin Transactions 1, no. 4, pp. 393-398. https://doi.org/10.1039/p19940000393

Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides. / Maeda, Yasuhiro; Shirai, Naohiro; Sato, Yoshiro.
In: Journal of the Chemical Society, Perkin Transactions 1, No. 4, 1994, p. 393-398.

Research output: Contribution to journal › Article › peer-review

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T1 - Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides

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AU - Shirai, Naohiro

AU - Sato, Yoshiro

PY - 1994

Y1 - 1994

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AB - N,N-Dimethyl(pyridylmethyl)ammonium N-methylides 2, 6, 11, N,N-dimethyl(1-methylpyrrolyl-methyl)ammonium N-methylides 15, 20 and N,N-dimethyl(1-methylindolylmethyl)ammonium N-methylides 23, 28 were generated by fluoride ion-induced desilylation of the corresponding (trimethylsilyl) methylammonium salts 1,5,10,14,19,22 and 27, and the isomerization products of the ylides were investigated.

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Maeda Y, Shirai N, Sato Y. Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides. Journal of the Chemical Society, Perkin Transactions 1. 1994;(4):393-398. doi: 10.1039/p19940000393

Chemical behaviour of trimethylammonium N-methylides substituted with nitrogen-containing heteroaromatic rings. Rearrangement of N,N-dimethyl- (pyridylmethyl)ammonium, N,N-dimethyl-(1-methylpyrrolylmethyl)ammonium and N,N-dimethyl-(1-methylindolylmethyl)ammonium N-methylides

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