Abstract
– A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.
| Original language | English |
|---|---|
| Pages (from-to) | 1157-1164 |
| Number of pages | 8 |
| Journal | Heterocycles |
| Volume | 97 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Jan 1 2018 |
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ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry
Cite this
Total sytnhesis of Rhoiptelol B. / Tanaka, Nobuhiro; Takamura, Hiroyoshi; Kadota, Isao.
In: Heterocycles, Vol. 97, No. 2, 01.01.2018, p. 1157-1164.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Total sytnhesis of Rhoiptelol B
AU - Tanaka, Nobuhiro
AU - Takamura, Hiroyoshi
AU - Kadota, Isao
PY - 2018/1/1
Y1 - 2018/1/1
N2 - – A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.
AB - – A stereoselective total synthesis of rhoiptelol B, a diarylheptanoid isolated from the fruits of Rhoiptelea chiliantha, is described. The tetrahydropyran ring was constructed via an intramolecular allylation methodology.
UR - http://www.scopus.com/inward/record.url?scp=85069613843&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85069613843&partnerID=8YFLogxK
U2 - 10.3987/COM-18-S(T)57
DO - 10.3987/COM-18-S(T)57
M3 - Article
AN - SCOPUS:85069613843
VL - 97
SP - 1157
EP - 1164
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 2
ER -