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 |
| Publication status | Published - 1985 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
Acyclic stereoselection. 32. Synthesis and characterization of the diastereomeric (4S)-pentane-1,2,3,4-tetrols. / Takai, Kazuhiko; Heathcock, Clayton H.
In: Journal of Organic Chemistry, Vol. 50, No. 18, 1985, p. 3247-3251.Research output: Contribution to journal › Article
}
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
Y1 - 1985
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.
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UR - http://www.scopus.com/inward/citedby.url?scp=0000414648&partnerID=8YFLogxK
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 -