Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems

Makoto Nitta; Nobuhiro Kanomata; Masaru Tada

doi:10.1016/S0040-4039(00)88788-2

Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems

Makoto Nitta^*, Nobuhiro Kanomata, Masaru Tada

^*Corresponding author for this work

School of Advanced Science and Engineering

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

10 Citations (Scopus)

Abstract

Novel 1-aza-6,11- and 1-aza-4,9-methnocyclopentacycloundecene ring systems were synthesized by the reaction of 3,8-methano[11]annulenone with N-(1-phenylvinylimino)triphenylphosphorane followed by dehydrogenation. These compounds are diatropic as 14pielectron vinylogues of 1-azaazulene.

Original language	English
Pages (from-to)	1291-1294
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	9
DOIs	https://doi.org/10.1016/S0040-4039(00)88788-2
Publication status	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems",

abstract = "Novel 1-aza-6,11- and 1-aza-4,9-methnocyclopentacycloundecene ring systems were synthesized by the reaction of 3,8-methano[11]annulenone with N-(1-phenylvinylimino)triphenylphosphorane followed by dehydrogenation. These compounds are diatropic as 14pielectron vinylogues of 1-azaazulene.",

author = "Makoto Nitta and Nobuhiro Kanomata and Masaru Tada",

year = "1990",

doi = "10.1016/S0040-4039(00)88788-2",

language = "English",

volume = "31",

pages = "1291--1294",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "9",

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TY - JOUR

T1 - Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems

AU - Nitta, Makoto

AU - Kanomata, Nobuhiro

AU - Tada, Masaru

PY - 1990

Y1 - 1990

N2 - Novel 1-aza-6,11- and 1-aza-4,9-methnocyclopentacycloundecene ring systems were synthesized by the reaction of 3,8-methano[11]annulenone with N-(1-phenylvinylimino)triphenylphosphorane followed by dehydrogenation. These compounds are diatropic as 14pielectron vinylogues of 1-azaazulene.

AB - Novel 1-aza-6,11- and 1-aza-4,9-methnocyclopentacycloundecene ring systems were synthesized by the reaction of 3,8-methano[11]annulenone with N-(1-phenylvinylimino)triphenylphosphorane followed by dehydrogenation. These compounds are diatropic as 14pielectron vinylogues of 1-azaazulene.

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U2 - 10.1016/S0040-4039(00)88788-2

DO - 10.1016/S0040-4039(00)88788-2

M3 - Article

AN - SCOPUS:0025034597

VL - 31

SP - 1291

EP - 1294

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 9

ER -

Synthesis and spectroscopic properties of 1-azamkthanocyclopentacycloundecene ring systems

Abstract

ASJC Scopus subject areas

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