Abstract
The tricycle (5) with two trans-fused angular methyl groups is constructed from tiglic aldehyde and (S)-carvone involving a stereocontrolled aldol reaction and an endo-selective intramolecular Diels-Alder (IMDA) reaction; the stereochemistry was established by an X-ray study.
| Original language | English |
|---|---|
| Pages (from-to) | 1294-1295 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 17 |
| DOIs | |
| Publication status | Published - 1989 Jan 1 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Molecular Medicine
Cite this
An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton. / Shing, Tony Kung Ming; Tang, Ying; Malone, John F.
In: Journal of the Chemical Society, Chemical Communications, No. 17, 01.01.1989, p. 1294-1295.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - An expeditious and enantioselective entry to the ABC ring of the quassinoid skeleton
AU - Shing, Tony Kung Ming
AU - Tang, Ying
AU - Malone, John F.
PY - 1989/1/1
Y1 - 1989/1/1
N2 - The tricycle (5) with two trans-fused angular methyl groups is constructed from tiglic aldehyde and (S)-carvone involving a stereocontrolled aldol reaction and an endo-selective intramolecular Diels-Alder (IMDA) reaction; the stereochemistry was established by an X-ray study.
AB - The tricycle (5) with two trans-fused angular methyl groups is constructed from tiglic aldehyde and (S)-carvone involving a stereocontrolled aldol reaction and an endo-selective intramolecular Diels-Alder (IMDA) reaction; the stereochemistry was established by an X-ray study.
UR - http://www.scopus.com/inward/record.url?scp=37049074473&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=37049074473&partnerID=8YFLogxK
U2 - 10.1039/C39890001294
DO - 10.1039/C39890001294
M3 - Article
AN - SCOPUS:37049074473
SP - 1294
EP - 1295
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 17
ER -