Rapid assembly of vinigrol's unique carbocyclic skeleton

Jason G.M. Morton; Cristian Draghici; Laura D. Kwon; Jon T. Njardarson

doi:10.1021/ol901519k

Rapid assembly of vinigrol's unique carbocyclic skeleton

Jason G.M. Morton, Cristian Draghici, Laura D. Kwon, Jon T. Njardarson

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

53 Scopus citations

Abstract

Detailed In this account are our efforts toward the total synthesis of vinigrol. A highly expedient and convergent synthetic approach made possible by the use of a strategic oxidative dearomatization reaction coupled with a series of ensuing substrate controlled transformations is discussed.

Original language	English (US)
Pages (from-to)	4492-4495
Number of pages	4
Journal	Organic Letters
Volume	11
Issue number	20
DOIs	https://doi.org/10.1021/ol901519k
State	Published - Oct 15 2009
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol901519k

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title = "Rapid assembly of vinigrol's unique carbocyclic skeleton",

abstract = "Detailed In this account are our efforts toward the total synthesis of vinigrol. A highly expedient and convergent synthetic approach made possible by the use of a strategic oxidative dearomatization reaction coupled with a series of ensuing substrate controlled transformations is discussed.",

author = "Morton, {Jason G.M.} and Cristian Draghici and Kwon, {Laura D.} and Njardarson, {Jon T.}",

year = "2009",

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doi = "10.1021/ol901519k",

language = "English (US)",

volume = "11",

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journal = "Organic Letters",

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T1 - Rapid assembly of vinigrol's unique carbocyclic skeleton

AU - Morton, Jason G.M.

AU - Draghici, Cristian

AU - Kwon, Laura D.

AU - Njardarson, Jon T.

PY - 2009/10/15

Y1 - 2009/10/15

N2 - Detailed In this account are our efforts toward the total synthesis of vinigrol. A highly expedient and convergent synthetic approach made possible by the use of a strategic oxidative dearomatization reaction coupled with a series of ensuing substrate controlled transformations is discussed.

AB - Detailed In this account are our efforts toward the total synthesis of vinigrol. A highly expedient and convergent synthetic approach made possible by the use of a strategic oxidative dearomatization reaction coupled with a series of ensuing substrate controlled transformations is discussed.

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JO - Organic Letters

JF - Organic Letters

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Rapid assembly of vinigrol's unique carbocyclic skeleton

Abstract

ASJC Scopus subject areas

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