Abstract
Total synthesis of maturone (1) by the regioselective Dials-Alder reaction of benzofuranquinone (7) is described. Compound (7) was easily obtained by an application of the fused furan constructing method using allenic sulfonium salt (3) and cyclic 1,3-dicarbonyl compound.
| Original language | English |
|---|---|
| Pages (from-to) | 33-36 |
| Number of pages | 4 |
| Journal | Heterocycles |
| Volume | 35 |
| Issue number | 1 |
| Publication status | Published - Jan 1 1993 |
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All Science Journal Classification (ASJC) codes
- Organic Chemistry
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Regioselective synthesis of maturone via Lewis acid catalyzed Diels-Alder reaction. / Aso, Mariko; Ojida, Akio; Yang, Guang; Kanematsu, Ken.
In: Heterocycles, Vol. 35, No. 1, 01.01.1993, p. 33-36.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Regioselective synthesis of maturone via Lewis acid catalyzed Diels-Alder reaction
AU - Aso, Mariko
AU - Ojida, Akio
AU - Yang, Guang
AU - Kanematsu, Ken
PY - 1993/1/1
Y1 - 1993/1/1
N2 - Total synthesis of maturone (1) by the regioselective Dials-Alder reaction of benzofuranquinone (7) is described. Compound (7) was easily obtained by an application of the fused furan constructing method using allenic sulfonium salt (3) and cyclic 1,3-dicarbonyl compound.
AB - Total synthesis of maturone (1) by the regioselective Dials-Alder reaction of benzofuranquinone (7) is described. Compound (7) was easily obtained by an application of the fused furan constructing method using allenic sulfonium salt (3) and cyclic 1,3-dicarbonyl compound.
UR - http://www.scopus.com/inward/record.url?scp=1542761358&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1542761358&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:1542761358
VL - 35
SP - 33
EP - 36
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 1
ER -