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

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

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

Access to Document

10.1039/p19940000393

Fingerprint

Dive into the research topics of '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'. Together they form a unique fingerprint.

Cite this

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.

@article{96ee72b379a046578c08b6c673e8b0cb,

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",

issn = "1472-7781",

publisher = "Chemical Society",

number = "4",

}

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

TY - JOUR

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

AU - Maeda, Yasuhiro

AU - Shirai, Naohiro

AU - Sato, Yoshiro

PY - 1994

Y1 - 1994

N2 - 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.

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.

UR - https://www.scopus.com/pages/publications/37049089613

UR - https://www.scopus.com/pages/publications/37049089613#tab=citedBy

U2 - 10.1039/p19940000393

DO - 10.1039/p19940000393

M3 - Article

AN - SCOPUS:37049089613

SN - 1472-7781

SP - 393

EP - 398

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

IS - 4

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this