4-aza-2,7-dimethyl-[1-<i>H</i>]cyclopropa[b]-naphthalene: the first nitrogen analogue of a cyclopropanaphthalene

Muller, Paul; Schaller, Jean-Pierre

doi:10.1016/S0040-4039(00)99503-0

Scientific article

Letter

English

4-aza-2,7-dimethyl-[1-H]cyclopropa[b]-naphthalene: the first nitrogen analogue of a cyclopropanaphthalene

ContributorsMuller, Paul; Schaller, Jean-Pierre

Published inTetrahedron Letters, vol. 30, no. 12, p. 1507-1510

Publication date1989

Abstract

The title compound 1 is synthesized via Diels-Alder addition of 4-aza-2,7-dimethyl-isobenzofuran (5) to 1,2-bromochlorocyclopropene and aromatization of the adduct 6 with low-valent titanium. The title compound 1 is synthesized by aromatization of the cycloadduct 6 of 4-aza-2,7-dimethyl-isobenzofuran 5 to 1,2-bromochlorocyclopropene with low-valent titanium.

Affiliation entities

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Funding

Swiss National Science Foundation - 2.602-0.87

Citation (ISO format)

MULLER, Paul, SCHALLER, Jean-Pierre. 4-aza-2,7-dimethyl-[1-H]cyclopropa[b]-naphthalene: the first nitrogen analogue of a cyclopropanaphthalene. In: Tetrahedron Letters, 1989, vol. 30, n° 12, p. 1507–1510. doi: 10.1016/S0040-4039(00)99503-0

Article (Published version)

Identifiers

PID : unige:152731
DOI : 10.1016/S0040-4039(00)99503-0

Additional URL for this publicationhttps://linkinghub.elsevier.com/retrieve/pii/S0040403900995030

Journal ISSN0040-4039

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4-aza-2,7-dimethyl-[1-H]cyclopropa[b]-naphthalene: the first nitrogen analogue of a cyclopropanaphthalene

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