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

54 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

Access to Document

10.1021/ol901519k

Cite this

@article{ce87eb4ace524336bbae47651f14c20c,

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",

month = oct,

day = "15",

doi = "10.1021/ol901519k",

language = "English (US)",

volume = "11",

pages = "4492--4495",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "20",

}

TY - JOUR

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.

UR - https://www.scopus.com/pages/publications/70349909599

UR - https://www.scopus.com/pages/publications/70349909599#tab=citedBy

U2 - 10.1021/ol901519k

DO - 10.1021/ol901519k

M3 - Article

C2 - 19728692

AN - SCOPUS:70349909599

SN - 1523-7060

VL - 11

SP - 4492

EP - 4495

JO - Organic Letters

JF - Organic Letters

IS - 20

ER -

Rapid assembly of vinigrol's unique carbocyclic skeleton

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this