A synthesis of (-)-mintlactone

Roderick W. Bates; S. Sridhar

doi:10.1021/jo801433f

A synthesis of (-)-mintlactone

Roderick W. Bates, S. Sridhar

Nanyang Technological University

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

30 Citations (Scopus)

Abstract

(Chemical Equation Presented) Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction.

Original language	English
Pages (from-to)	8104-8105
Number of pages	2
Journal	Journal of Organic Chemistry
Volume	73
Issue number	20
DOIs	https://doi.org/10.1021/jo801433f
Publication status	Published - Oct 17 2008
Externally published	Yes

ASJC Scopus Subject Areas

Organic Chemistry

Access to Document

10.1021/jo801433f

Cite this

@article{85c8aa3cc53a4e3da48281c6aa807a21,

title = "A synthesis of (-)-mintlactone",

abstract = "(Chemical Equation Presented) Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction.",

author = "Bates, {Roderick W.} and S. Sridhar",

year = "2008",

month = oct,

day = "17",

doi = "10.1021/jo801433f",

language = "English",

volume = "73",

pages = "8104--8105",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "20",

}

TY - JOUR

T1 - A synthesis of (-)-mintlactone

AU - Bates, Roderick W.

AU - Sridhar, S.

PY - 2008/10/17

Y1 - 2008/10/17

N2 - (Chemical Equation Presented) Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction.

AB - (Chemical Equation Presented) Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction.

UR - http://www.scopus.com/inward/record.url?scp=53849127188&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=53849127188&partnerID=8YFLogxK

U2 - 10.1021/jo801433f

DO - 10.1021/jo801433f

M3 - Article

C2 - 18811204

AN - SCOPUS:53849127188

SN - 0022-3263

VL - 73

SP - 8104

EP - 8105

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 20

ER -

A synthesis of (-)-mintlactone

Abstract

ASJC Scopus Subject Areas

Access to Document

Other files and links

Fingerprint

Cite this