Abstract
Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.
| Original language | English |
|---|---|
| Pages (from-to) | 383-386 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 25 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1984 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone. / Posner, Gary H.; Kogan, Timothy P.; Hulce, Martin.
In: Tetrahedron Letters, Vol. 25, No. 4, 1984, p. 383-386.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.
AU - Posner, Gary H.
AU - Kogan, Timothy P.
AU - Hulce, Martin
PY - 1984
Y1 - 1984
N2 - Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.
AB - Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.
UR - http://www.scopus.com/inward/record.url?scp=0000153005&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0000153005&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)99889-7
DO - 10.1016/S0040-4039(00)99889-7
M3 - Article
VL - 25
SP - 383
EP - 386
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 4
ER -