Abstract
In the presence of triethylamine, the Diels-Alder reaction of 3-hydroxy-2-pyrones with 1,4-naphthoquinones by a decarboxylation-oxidation process gave anthraquinone derivatives in good to excellent yields.
| Original language | English |
|---|---|
| Article number | U28605ST |
| Pages (from-to) | 124-126 |
| Number of pages | 3 |
| Journal | Synlett |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 5 2006 |
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Keywords
- 3-Hydroxy-2-pyrone
- Anthraquinone
- Diels-Alder reactions
- Oxidations
- Tandem reactions
ASJC Scopus subject areas
- Organic Chemistry
Cite this
Synthesis of anthraquinone derivatives : Tandem Diels-Alder-decarboxylation- oxidation reaction of 3-hydroxy-2-pyrone with 1,4-naphthoquinone. / Komiyama, Takuzo; Takaguchi, Yutaka; Tsuboi, Sadao.
In: Synlett, No. 1, U28605ST, 05.01.2006, p. 124-126.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis of anthraquinone derivatives
T2 - Tandem Diels-Alder-decarboxylation- oxidation reaction of 3-hydroxy-2-pyrone with 1,4-naphthoquinone
AU - Komiyama, Takuzo
AU - Takaguchi, Yutaka
AU - Tsuboi, Sadao
PY - 2006/1/5
Y1 - 2006/1/5
N2 - In the presence of triethylamine, the Diels-Alder reaction of 3-hydroxy-2-pyrones with 1,4-naphthoquinones by a decarboxylation-oxidation process gave anthraquinone derivatives in good to excellent yields.
AB - In the presence of triethylamine, the Diels-Alder reaction of 3-hydroxy-2-pyrones with 1,4-naphthoquinones by a decarboxylation-oxidation process gave anthraquinone derivatives in good to excellent yields.
KW - 3-Hydroxy-2-pyrone
KW - Anthraquinone
KW - Diels-Alder reactions
KW - Oxidations
KW - Tandem reactions
UR - http://www.scopus.com/inward/record.url?scp=30544440546&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=30544440546&partnerID=8YFLogxK
U2 - 10.1055/s-2005-922769
DO - 10.1055/s-2005-922769
M3 - Article
AN - SCOPUS:30544440546
SP - 124
EP - 126
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 1
M1 - U28605ST
ER -