The reaction of β-ketoacids with allylboronates

George Kabalka, Kathy Yang, Zhe Wang

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Allylboronates react with β-ketoacids to yield tertiary homoallylic β-hydroxycarboxylic acids. The reaction presumably proceeds via a bicyclic transition state. The β-carboxylic substituent enhances the rate of the reaction.

Original languageEnglish (US)
Pages (from-to)511-517
Number of pages7
JournalSynthetic Communications
Volume31
Issue number4
DOIs
StatePublished - Jan 1 2001
Externally publishedYes

Fingerprint

Acids

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

The reaction of β-ketoacids with allylboronates. / Kabalka, George; Yang, Kathy; Wang, Zhe.

In: Synthetic Communications, Vol. 31, No. 4, 01.01.2001, p. 511-517.

Research output: Contribution to journalArticle

Kabalka, George ; Yang, Kathy ; Wang, Zhe. / The reaction of β-ketoacids with allylboronates. In: Synthetic Communications. 2001 ; Vol. 31, No. 4. pp. 511-517.
@article{143f1d470aa0486ea146f581e525faf5,
title = "The reaction of β-ketoacids with allylboronates",
abstract = "Allylboronates react with β-ketoacids to yield tertiary homoallylic β-hydroxycarboxylic acids. The reaction presumably proceeds via a bicyclic transition state. The β-carboxylic substituent enhances the rate of the reaction.",
author = "George Kabalka and Kathy Yang and Zhe Wang",
year = "2001",
month = "1",
day = "1",
doi = "10.1081/SCC-100000576",
language = "English (US)",
volume = "31",
pages = "511--517",
journal = "Synthetic Communications",
issn = "0039-7911",
publisher = "Taylor and Francis Ltd.",
number = "4",

}

TY - JOUR

T1 - The reaction of β-ketoacids with allylboronates

AU - Kabalka, George

AU - Yang, Kathy

AU - Wang, Zhe

PY - 2001/1/1

Y1 - 2001/1/1

N2 - Allylboronates react with β-ketoacids to yield tertiary homoallylic β-hydroxycarboxylic acids. The reaction presumably proceeds via a bicyclic transition state. The β-carboxylic substituent enhances the rate of the reaction.

AB - Allylboronates react with β-ketoacids to yield tertiary homoallylic β-hydroxycarboxylic acids. The reaction presumably proceeds via a bicyclic transition state. The β-carboxylic substituent enhances the rate of the reaction.

UR - http://www.scopus.com/inward/record.url?scp=0035004812&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035004812&partnerID=8YFLogxK

U2 - 10.1081/SCC-100000576

DO - 10.1081/SCC-100000576

M3 - Article

VL - 31

SP - 511

EP - 517

JO - Synthetic Communications

JF - Synthetic Communications

SN - 0039-7911

IS - 4

ER -