Knoevenagel condensations of β-hemiacetyl esters

Pilho Kim; Marilyn M. Olmstead; Michael H. Nantz; Mark J. Kurth

Knoevenagel condensations of β-hemiacetyl esters

Pilho Kim, Marilyn M. Olmstead, Michael H. Nantz, Mark J. Kurth

Chemistry

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

14 Scopus citations

Abstract

The intermolecular Knoevenagel condensation of β-hemiacetyl ester proceeds by an in situ unmasking of a reactive ω-hydroxy-β-keto ester giving unsaturated ω-hydroxy-β-keto esters 6-12 which accommodate acetal formation. (C) 2000 Elsevier Science Ltd.

Original language	English (US)
Pages (from-to)	4029-4032
Number of pages	4
Journal	Tetrahedron Letters
Volume	41
Issue number	21
State	Published - May 29 2000

Keywords

Acetal formation
Eleuthesides
Knoevenagel condensation

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Fingerprint Dive into the research topics of 'Knoevenagel condensations of β-hemiacetyl esters'. Together they form a unique fingerprint.

Cite this

@article{de571efacb2f4e0b9310c79b09b7a996,

title = "Knoevenagel condensations of β-hemiacetyl esters",

abstract = "The intermolecular Knoevenagel condensation of β-hemiacetyl ester proceeds by an in situ unmasking of a reactive ω-hydroxy-β-keto ester giving unsaturated ω-hydroxy-β-keto esters 6-12 which accommodate acetal formation. (C) 2000 Elsevier Science Ltd.",

keywords = "Acetal formation, Eleuthesides, Knoevenagel condensation",

author = "Pilho Kim and Olmstead, {Marilyn M.} and Nantz, {Michael H.} and Kurth, {Mark J.}",

year = "2000",

month = may,

day = "29",

language = "English (US)",

volume = "41",

pages = "4029--4032",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "21",

}

TY - JOUR

T1 - Knoevenagel condensations of β-hemiacetyl esters

AU - Kim, Pilho

AU - Olmstead, Marilyn M.

AU - Nantz, Michael H.

AU - Kurth, Mark J.

PY - 2000/5/29

Y1 - 2000/5/29

N2 - The intermolecular Knoevenagel condensation of β-hemiacetyl ester proceeds by an in situ unmasking of a reactive ω-hydroxy-β-keto ester giving unsaturated ω-hydroxy-β-keto esters 6-12 which accommodate acetal formation. (C) 2000 Elsevier Science Ltd.

AB - The intermolecular Knoevenagel condensation of β-hemiacetyl ester proceeds by an in situ unmasking of a reactive ω-hydroxy-β-keto ester giving unsaturated ω-hydroxy-β-keto esters 6-12 which accommodate acetal formation. (C) 2000 Elsevier Science Ltd.

KW - Acetal formation

KW - Eleuthesides

KW - Knoevenagel condensation

UR - http://www.scopus.com/inward/record.url?scp=0034729316&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034729316&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0034729316

VL - 41

SP - 4029

EP - 4032

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 21

ER -

Knoevenagel condensations of β-hemiacetyl esters

Abstract

Keywords

ASJC Scopus subject areas

Other files and links

Cite this