A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene

Martin G. Banwell; Mark J. Coster; Ochitha P. Karunaratne; Jason A. Smith

doi:10.1039/b205230j

A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene

Martin G. Banwell^*, Mark J. Coster, Ochitha P. Karunaratne, Jason A. Smith

^*Corresponding author for this work

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

24 Citations (Scopus)

Abstract

The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, has been converted, via a sequence of reactions including oxidative C – C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (1).

Original language	English
Pages (from-to)	1622-1624
Number of pages	3
Journal	Journal of the Chemical Society, Perkin Transactions 1
Volume	2
Issue number	14
DOIs	https://doi.org/10.1039/b205230j
Publication status	Published - 29 May 2002

Access to Document

10.1039/b205230j

Cite this

@article{582fc952098d4d9faa03a95851e28ec5,

title = "A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene",

abstract = "The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, has been converted, via a sequence of reactions including oxidative C – C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (1).",

author = "Banwell, \{Martin G.\} and Coster, \{Mark J.\} and Karunaratne, \{Ochitha P.\} and Smith, \{Jason A.\}",

year = "2002",

month = may,

day = "29",

doi = "10.1039/b205230j",

language = "English",

volume = "2",

pages = "1622--1624",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

issn = "1472-7781",

publisher = "Chemical Society",

number = "14",

}

TY - JOUR

T1 - A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene

AU - Banwell, Martin G.

AU - Coster, Mark J.

AU - Karunaratne, Ochitha P.

AU - Smith, Jason A.

PY - 2002/5/29

Y1 - 2002/5/29

N2 - The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, has been converted, via a sequence of reactions including oxidative C – C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (1).

AB - The enantiomerically pure cis-1,2-diol 2, which is obtained by microbial oxidation of naphthalene, has been converted, via a sequence of reactions including oxidative C – C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (1).

UR - https://www.scopus.com/pages/publications/0035996938

U2 - 10.1039/b205230j

DO - 10.1039/b205230j

M3 - Article

SN - 1472-7781

VL - 2

SP - 1622

EP - 1624

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

IS - 14

ER -

A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene

Abstract

Access to Document

Other files and links

Fingerprint

Cite this