Doubly diastereoselective iodolactonizations: Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations

John C. McKew; Marilyn M. Olmstead; Mark J. Kurth

Doubly diastereoselective iodolactonizations: Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations

John C. McKew, Marilyn M. Olmstead, Mark J. Kurth

Chemistry

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

11 Scopus citations

Abstract

Nonracemic nonadienoic acids (v) were subjected to iodolactonization conditions and, by doubly diastereoselective cyclization, delivered enantiomerically pure iodo lactones replete with up to five contiguous stereogenic centers.

Original language	English (US)
Pages (from-to)	3389-3393
Number of pages	5
Journal	Journal of Organic Chemistry
Volume	59
Issue number	12
State	Published - 1994

ASJC Scopus subject areas

Organic Chemistry

Cite this

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title = "Doubly diastereoselective iodolactonizations: Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations",

abstract = "Nonracemic nonadienoic acids (v) were subjected to iodolactonization conditions and, by doubly diastereoselective cyclization, delivered enantiomerically pure iodo lactones replete with up to five contiguous stereogenic centers.",

author = "McKew, {John C.} and Olmstead, {Marilyn M.} and Kurth, {Mark J.}",

year = "1994",

language = "English (US)",

volume = "59",

pages = "3389--3393",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "12",

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T1 - Doubly diastereoselective iodolactonizations

T2 - Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations

AU - McKew, John C.

AU - Olmstead, Marilyn M.

AU - Kurth, Mark J.

PY - 1994

Y1 - 1994

N2 - Nonracemic nonadienoic acids (v) were subjected to iodolactonization conditions and, by doubly diastereoselective cyclization, delivered enantiomerically pure iodo lactones replete with up to five contiguous stereogenic centers.

AB - Nonracemic nonadienoic acids (v) were subjected to iodolactonization conditions and, by doubly diastereoselective cyclization, delivered enantiomerically pure iodo lactones replete with up to five contiguous stereogenic centers.

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M3 - Article

AN - SCOPUS:0000065780

VL - 59

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EP - 3393

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 12

ER -

Doubly diastereoselective iodolactonizations: Olefin and face selectivity in nona-2,7-diene-5-carboxylic acid cyclizations

Abstract

ASJC Scopus subject areas

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