Abstract
Ynolates react with isocyanates to give azetidine-2,4-diones via a [2+2] type cycloaddition. The [4+2] type cycloaddition proceeds in the reactions of vinyl isocyanates with ynolates to provide 2-pyridones.
| Original language | English |
|---|---|
| Pages (from-to) | 39-43 |
| Number of pages | 5 |
| Journal | Heterocycles |
| Volume | 66 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Dec 31 2005 |
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All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Pharmacology
- Organic Chemistry
Cite this
[2+2] and [2+4] type cycloadditions of isocyanates with ynolates. / Shindo, Mitsuru; Harada, Akiko; Matsumoto, Kenji; Shishido, Kozo.
In: Heterocycles, Vol. 66, No. 1, 31.12.2005, p. 39-43.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - [2+2] and [2+4] type cycloadditions of isocyanates with ynolates
AU - Shindo, Mitsuru
AU - Harada, Akiko
AU - Matsumoto, Kenji
AU - Shishido, Kozo
PY - 2005/12/31
Y1 - 2005/12/31
N2 - Ynolates react with isocyanates to give azetidine-2,4-diones via a [2+2] type cycloaddition. The [4+2] type cycloaddition proceeds in the reactions of vinyl isocyanates with ynolates to provide 2-pyridones.
AB - Ynolates react with isocyanates to give azetidine-2,4-diones via a [2+2] type cycloaddition. The [4+2] type cycloaddition proceeds in the reactions of vinyl isocyanates with ynolates to provide 2-pyridones.
UR - http://www.scopus.com/inward/record.url?scp=33646862816&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33646862816&partnerID=8YFLogxK
U2 - 10.3987/COM-05-S(K)9
DO - 10.3987/COM-05-S(K)9
M3 - Article
AN - SCOPUS:33646862816
VL - 66
SP - 39
EP - 43
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 1
ER -