Abstract
An approach to the enantiospecific syntheses of sesbanimide and its enantiomer is described; enantiomeric intermediates in the syntheses of both compounds possessing the required glutarimide and 1,3-dioxane rings are derived from D-glucose.
| Original language | English |
|---|---|
| Pages (from-to) | 835-837 |
| Number of pages | 3 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 13 |
| Publication status | Published - 1984 Dec 1 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Molecular Medicine
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An approach to the enantiospecific syntheses of sesbanimide and its enantiomer from D-glucose. / Fleet, George W.J.; Shing, Tony Kung Ming.
In: Journal of the Chemical Society, Chemical Communications, No. 13, 01.12.1984, p. 835-837.Research output: Contribution to journal › Article
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TY - JOUR
T1 - An approach to the enantiospecific syntheses of sesbanimide and its enantiomer from D-glucose
AU - Fleet, George W.J.
AU - Shing, Tony Kung Ming
PY - 1984/12/1
Y1 - 1984/12/1
N2 - An approach to the enantiospecific syntheses of sesbanimide and its enantiomer is described; enantiomeric intermediates in the syntheses of both compounds possessing the required glutarimide and 1,3-dioxane rings are derived from D-glucose.
AB - An approach to the enantiospecific syntheses of sesbanimide and its enantiomer is described; enantiomeric intermediates in the syntheses of both compounds possessing the required glutarimide and 1,3-dioxane rings are derived from D-glucose.
UR - http://www.scopus.com/inward/record.url?scp=37049092577&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=37049092577&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:37049092577
SP - 835
EP - 837
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 13
ER -