Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins

Martin G. Banwell; Andrew T. Phillis; Anthony C. Willis

doi:10.1021/ol062224d

Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins

Martin G. Banwell^*, Andrew T. Phillis, Anthony C. Willis

^*Corresponding author for this work

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

23 Citations (Scopus)

Abstract

The readily available hexahydrofluorene 5 has been elaborated over six steps, including three involving cyclopropane ring-cleavage reactions, into compound 12 which incorporates the carbocyclic framework associated with gibberellins.

Original language	English
Pages (from-to)	5341-5344
Number of pages	4
Journal	Organic Letters
Volume	8
Issue number	23
DOIs	https://doi.org/10.1021/ol062224d
Publication status	Published - 9 Nov 2006

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title = "Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins",

abstract = "The readily available hexahydrofluorene 5 has been elaborated over six steps, including three involving cyclopropane ring-cleavage reactions, into compound 12 which incorporates the carbocyclic framework associated with gibberellins.",

author = "Banwell, {Martin G.} and Phillis, {Andrew T.} and Willis, {Anthony C.}",

year = "2006",

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doi = "10.1021/ol062224d",

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journal = "Organic Letters",

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T1 - Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins

AU - Banwell, Martin G.

AU - Phillis, Andrew T.

AU - Willis, Anthony C.

PY - 2006/11/9

Y1 - 2006/11/9

N2 - The readily available hexahydrofluorene 5 has been elaborated over six steps, including three involving cyclopropane ring-cleavage reactions, into compound 12 which incorporates the carbocyclic framework associated with gibberellins.

AB - The readily available hexahydrofluorene 5 has been elaborated over six steps, including three involving cyclopropane ring-cleavage reactions, into compound 12 which incorporates the carbocyclic framework associated with gibberellins.

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U2 - 10.1021/ol062224d

DO - 10.1021/ol062224d

M3 - Article

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JO - Organic Letters

JF - Organic Letters

IS - 23

ER -

Exploitation of cyclopropane ring-cleavage reactions for the rapid assembly of tetracyclic frameworks related to gibberellins

Abstract

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