Enantiomerically pure acetals in organic synthesis. 3. A synthesis of (R)-mevalonic acid lactone

Eugene A Mash, Jeffrey B. Arterburn

Research output: Contribution to journalArticle

18 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)885-888
Number of pages4
JournalJournal of Organic Chemistry
Volume56
Issue number2
StatePublished - 1991

Fingerprint

Acetals
mevalonolactone

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Enantiomerically pure acetals in organic synthesis. 3. A synthesis of (R)-mevalonic acid lactone. / Mash, Eugene A; Arterburn, Jeffrey B.

In: Journal of Organic Chemistry, Vol. 56, No. 2, 1991, p. 885-888.

Research output: Contribution to journalArticle

@article{d6e4b86ba23644c8983318a07ac3ab01,
title = "Enantiomerically pure acetals in organic synthesis. 3. A synthesis of (R)-mevalonic acid lactone",
author = "Mash, {Eugene A} and Arterburn, {Jeffrey B.}",
year = "1991",
language = "English (US)",
volume = "56",
pages = "885--888",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "2",

}

TY - JOUR

T1 - Enantiomerically pure acetals in organic synthesis. 3. A synthesis of (R)-mevalonic acid lactone

AU - Mash, Eugene A

AU - Arterburn, Jeffrey B.

PY - 1991

Y1 - 1991

UR - http://www.scopus.com/inward/record.url?scp=0008518205&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0008518205&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0008518205

VL - 56

SP - 885

EP - 888

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 2

ER -