Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones
A convenient synthesis of 4-hydroxy spiro[4.n]alk-2-ene-1-ones and spiro [4.n] alk-2-ene-1,4-diones, which involves the intramolecular acylation of α-sulfinyl carbanions followed by pyrolysis and/or oxidation, is described. © 1989.
محفوظ في:
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| التنسيق: | مقال |
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2018
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| الوصول للمادة أونلاين: | https://repository.li.mahidol.ac.th/handle/123456789/15721 |
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th-mahidol.157212018-06-14T16:17:30Z Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones Manat Pohmakotr Supatara Popuang Sirirat Chancharunee Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A convenient synthesis of 4-hydroxy spiro[4.n]alk-2-ene-1-ones and spiro [4.n] alk-2-ene-1,4-diones, which involves the intramolecular acylation of α-sulfinyl carbanions followed by pyrolysis and/or oxidation, is described. © 1989. 2018-06-14T09:12:53Z 2018-06-14T09:12:53Z 1989-01-01 Article Tetrahedron Letters. Vol.30, No.13 (1989), 1715-1718 10.1016/S0040-4039(00)99563-7 00404039 2-s2.0-0000598807 https://repository.li.mahidol.ac.th/handle/123456789/15721 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0000598807&origin=inward |
| institution |
Mahidol University |
| building |
Mahidol University Library |
| continent |
Asia |
| country |
Thailand Thailand |
| content_provider |
Mahidol University Library |
| collection |
Mahidol University Institutional Repository |
| topic |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics |
| spellingShingle |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Manat Pohmakotr Supatara Popuang Sirirat Chancharunee Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| description |
A convenient synthesis of 4-hydroxy spiro[4.n]alk-2-ene-1-ones and spiro [4.n] alk-2-ene-1,4-diones, which involves the intramolecular acylation of α-sulfinyl carbanions followed by pyrolysis and/or oxidation, is described. © 1989. |
| author2 |
Mahidol University |
| author_facet |
Mahidol University Manat Pohmakotr Supatara Popuang Sirirat Chancharunee |
| format |
Article |
| author |
Manat Pohmakotr Supatara Popuang Sirirat Chancharunee |
| author_sort |
Manat Pohmakotr |
| title |
Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| title_short |
Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| title_full |
Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| title_fullStr |
Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| title_full_unstemmed |
Intramolecular acylation of α-sulfinyl carbanions. A simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| title_sort |
intramolecular acylation of α-sulfinyl carbanions. a simple preparation of 4-oxygenated spiro[4.n]alk-2-ene-1-ones |
| publishDate |
2018 |
| url |
https://repository.li.mahidol.ac.th/handle/123456789/15721 |
| _version_ |
1763489772441960448 |