Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives

Paul G. Gassman; Lushi Tan; Thomas R. Hoye

doi:10.1016/0040-4039(95)02213-9

Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives

Paul G. Gassman
, Lushi Tan
, Thomas R. Hoye

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

15 Scopus citations

Abstract

The electrocyclic opening of dibromocyclopropane derivatives containing a tethered diene unit provides a good route to trienic cyclopentane derivatives. In one instance a bicyclic product arising from a formal 4 + 2 cycloaddition process was observed.

Original language	English (US)
Pages (from-to)	439-442
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	4
DOIs	https://doi.org/10.1016/0040-4039(95)02213-9
State	Published - Jan 22 1996

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Copyright 2017 Elsevier B.V., All rights reserved.

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title = "Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives",

abstract = "The electrocyclic opening of dibromocyclopropane derivatives containing a tethered diene unit provides a good route to trienic cyclopentane derivatives. In one instance a bicyclic product arising from a formal 4 + 2 cycloaddition process was observed.",

author = "Gassman, \{Paul G.\} and Lushi Tan and Hoye, \{Thomas R.\}",

year = "1996",

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T1 - Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives

AU - Gassman, Paul G.

AU - Tan, Lushi

AU - Hoye, Thomas R.

PY - 1996/1/22

Y1 - 1996/1/22

N2 - The electrocyclic opening of dibromocyclopropane derivatives containing a tethered diene unit provides a good route to trienic cyclopentane derivatives. In one instance a bicyclic product arising from a formal 4 + 2 cycloaddition process was observed.

AB - The electrocyclic opening of dibromocyclopropane derivatives containing a tethered diene unit provides a good route to trienic cyclopentane derivatives. In one instance a bicyclic product arising from a formal 4 + 2 cycloaddition process was observed.

UR - https://www.scopus.com/pages/publications/0030058852

UR - https://www.scopus.com/pages/publications/0030058852#tab=citedBy

U2 - 10.1016/0040-4039(95)02213-9

DO - 10.1016/0040-4039(95)02213-9

M3 - Article

AN - SCOPUS:0030058852

SN - 0040-4039

VL - 37

SP - 439

EP - 442

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 4

ER -

Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives

Abstract

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