Acyclic Stereoselection. 32. Synthesis and Characterization of the Diastereomeric (4S)-Pentane-1,2,3,4-tetrols

Kazuhiko Takai; Clayton H. Heathcock

doi:10.1021/jo00218a001

Acyclic Stereoselection. 32. Synthesis and Characterization of the Diastereomeric (4S)-Pentane-1,2,3,4-tetrols

Kazuhiko Takai, Clayton H. Heathcock

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

105 Citations (Scopus)

Abstract

The stereochemistry of the reaction of the lithium enolate of ester 1 and ketene acetal 3 with aldehyde 2 has been investigated. The diastereomeric (4S)-pentane-1,2,3,4-tetrols and their corresponding tetraacetate esters have been prepared and characterized.

Original language	English
Pages (from-to)	3247-3251
Number of pages	5
Journal	Journal of Organic Chemistry
Volume	50
Issue number	18
DOIs	https://doi.org/10.1021/jo00218a001
Publication status	Published - Jan 1 1985
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

Access to Document

10.1021/jo00218a001

Fingerprint Dive into the research topics of 'Acyclic Stereoselection. 32. Synthesis and Characterization of the Diastereomeric (4S)-Pentane-1,2,3,4-tetrols'. Together they form a unique fingerprint.

Cite this

@article{75086c367b47424cbf6c5126f6cd1018,

title = "Acyclic Stereoselection. 32. Synthesis and Characterization of the Diastereomeric (4S)-Pentane-1,2,3,4-tetrols",

abstract = "The stereochemistry of the reaction of the lithium enolate of ester 1 and ketene acetal 3 with aldehyde 2 has been investigated. The diastereomeric (4S)-pentane-1,2,3,4-tetrols and their corresponding tetraacetate esters have been prepared and characterized.",

author = "Kazuhiko Takai and Heathcock, {Clayton H.}",

year = "1985",

month = jan,

day = "1",

doi = "10.1021/jo00218a001",

language = "English",

volume = "50",

pages = "3247--3251",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "18",

}

TY - JOUR

T1 - Acyclic Stereoselection. 32. Synthesis and Characterization of the Diastereomeric (4S)-Pentane-1,2,3,4-tetrols

AU - Takai, Kazuhiko

AU - Heathcock, Clayton H.

PY - 1985/1/1

Y1 - 1985/1/1

N2 - The stereochemistry of the reaction of the lithium enolate of ester 1 and ketene acetal 3 with aldehyde 2 has been investigated. The diastereomeric (4S)-pentane-1,2,3,4-tetrols and their corresponding tetraacetate esters have been prepared and characterized.

AB - The stereochemistry of the reaction of the lithium enolate of ester 1 and ketene acetal 3 with aldehyde 2 has been investigated. The diastereomeric (4S)-pentane-1,2,3,4-tetrols and their corresponding tetraacetate esters have been prepared and characterized.

UR - http://www.scopus.com/inward/record.url?scp=0000414648&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000414648&partnerID=8YFLogxK

U2 - 10.1021/jo00218a001

DO - 10.1021/jo00218a001

M3 - Article

AN - SCOPUS:0000414648

VL - 50

SP - 3247

EP - 3251

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 18

ER -