Aromatization of Tetrahydrocyclopropa[α]naphthalenes: an Alternative Synthesis of 1H-Cyclopropa[α]naphthalene

Muller, Paul; Bernardinelli, Gérald Hugues; Godoy-Nguyen Thi, Huong Can

doi:10.1002/hlca.19890720723

Scientific article

English

Aromatization of Tetrahydrocyclopropa[α]naphthalenes: an Alternative Synthesis of 1H-Cyclopropa[α]naphthalene

ContributorsMuller, Paul; Bernardinelli, Gérald Hugues; Godoy-Nguyen Thi, Huong Can

Published inHelvetica Chimica Acta, vol. 72, no. 7, p. 1627-1638

Publication date1989

Abstract

1H-Cyclopropa[α]naphthalene (1a) is accessible via reduction of the dichloro compound 1c with LiAlH₄/AlCl₃. Several derivatives of tetrahydrocyclopropa[α]naphthalene were synthesized. However, contrary to their 1,1-dihalogeno analogues, they afforded no cycloproparenes upon attempted aromatization.

Affiliation entities

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

Citation (ISO format)

MULLER, Paul, BERNARDINELLI, Gérald Hugues, GODOY-NGUYEN THI, Huong Can. Aromatization of Tetrahydrocyclopropa[α]naphthalenes: an Alternative Synthesis of 1H-Cyclopropa[α]naphthalene. In: Helvetica Chimica Acta, 1989, vol. 72, n° 7, p. 1627–1638. doi: 10.1002/hlca.19890720723

Article (Published version)

Identifiers

PID : unige:152895
DOI : 10.1002/hlca.19890720723

Additional URL for this publicationhttps://onlinelibrary.wiley.com/doi/10.1002/hlca.19890720723

Journal ISSN0018-019X

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Aromatization of Tetrahydrocyclopropa[α]naphthalenes: an Alternative Synthesis of 1H-Cyclopropa[α]naphthalene

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