Abstract
In the presence of triethylamine, Diels-Alder reaction, involving decarboxylation-oxidation reaction of 3-hydroxy-2-pyrones with 1,4-benzoquinones gave 5-hydroxy-1,4-naphthoquinone derivatives in excellent to reasonable yields.
| Original language | English |
|---|---|
| Pages (from-to) | 1405-1407 |
| Number of pages | 3 |
| Journal | Synthesis |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - May 3 2006 |
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Keywords
- Diels-Alder reaction
- Oxidations
- Polycycles
- Quinones
- Tandem reaction
ASJC Scopus subject areas
- Organic Chemistry
Cite this
Effective one-pot synthesis of 5-hydroxy-1,4-naphthoquinone derivatives. / Komiyama, Takuzo; Takaguchi, Yutaka; Tsuboi, Sadao.
In: Synthesis, No. 9, 03.05.2006, p. 1405-1407.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Effective one-pot synthesis of 5-hydroxy-1,4-naphthoquinone derivatives
AU - Komiyama, Takuzo
AU - Takaguchi, Yutaka
AU - Tsuboi, Sadao
PY - 2006/5/3
Y1 - 2006/5/3
N2 - In the presence of triethylamine, Diels-Alder reaction, involving decarboxylation-oxidation reaction of 3-hydroxy-2-pyrones with 1,4-benzoquinones gave 5-hydroxy-1,4-naphthoquinone derivatives in excellent to reasonable yields.
AB - In the presence of triethylamine, Diels-Alder reaction, involving decarboxylation-oxidation reaction of 3-hydroxy-2-pyrones with 1,4-benzoquinones gave 5-hydroxy-1,4-naphthoquinone derivatives in excellent to reasonable yields.
KW - Diels-Alder reaction
KW - Oxidations
KW - Polycycles
KW - Quinones
KW - Tandem reaction
UR - http://www.scopus.com/inward/record.url?scp=33646569130&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33646569130&partnerID=8YFLogxK
U2 - 10.1055/s-2006-926417
DO - 10.1055/s-2006-926417
M3 - Article
AN - SCOPUS:33646569130
SP - 1405
EP - 1407
JO - Synthesis
JF - Synthesis
SN - 0039-7881
IS - 9
ER -