Abstract
The synthesis of (4S,5R)‐sitophilure (9a) was achieved from methyl 2‐methyl‐3‐oxopentanoate (1) via optical resolution of (±)‐6.
| Original language | English |
|---|---|
| Pages (from-to) | 899-902 |
| Number of pages | 4 |
| Journal | Liebigs Annalen der Chemie |
| Volume | 1988 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 1988 |
| Externally published | Yes |
Fingerprint
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
Pheromone synthesis, CX. Synthesis of (4S,5R)‐5‐hydroxy‐4‐methyl‐3‐heptanone (Sitophilure), the aggregation pheromone of Sitophilus oryzae and S. zeamais. / Mori, Kenji; Yoshimura, Toru; Sugai, Takeshi.
In: Liebigs Annalen der Chemie, Vol. 1988, No. 9, 1988, p. 899-902.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Pheromone synthesis, CX. Synthesis of (4S,5R)‐5‐hydroxy‐4‐methyl‐3‐heptanone (Sitophilure), the aggregation pheromone of Sitophilus oryzae and S. zeamais
AU - Mori, Kenji
AU - Yoshimura, Toru
AU - Sugai, Takeshi
PY - 1988
Y1 - 1988
N2 - The synthesis of (4S,5R)‐sitophilure (9a) was achieved from methyl 2‐methyl‐3‐oxopentanoate (1) via optical resolution of (±)‐6.
AB - The synthesis of (4S,5R)‐sitophilure (9a) was achieved from methyl 2‐methyl‐3‐oxopentanoate (1) via optical resolution of (±)‐6.
UR - http://www.scopus.com/inward/record.url?scp=84985283138&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84985283138&partnerID=8YFLogxK
U2 - 10.1002/jlac.198819880914
DO - 10.1002/jlac.198819880914
M3 - Article
AN - SCOPUS:84985283138
VL - 1988
SP - 899
EP - 902
JO - Annalen der Pharmacie
JF - Annalen der Pharmacie
SN - 0365-5490
IS - 9
ER -