A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions
A convenient and general synthetic method for spiro[4.n]alk-2-ene-1,6- diones and spiro[5.n]alk-2-ene-1,7-diones, which involves the intramolecular acylation of an α-sulfinyl carbanion, is described.
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| التنسيق: | مقال |
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2018
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th-mahidol.258802018-09-07T16:26:04Z A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions Manat Pohmakotr Tanasri Bunlaksananusorn Patoomratana Tuchinda Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics A convenient and general synthetic method for spiro[4.n]alk-2-ene-1,6- diones and spiro[5.n]alk-2-ene-1,7-diones, which involves the intramolecular acylation of an α-sulfinyl carbanion, is described. 2018-09-07T09:08:44Z 2018-09-07T09:08:44Z 2000-01-15 Article Tetrahedron Letters. Vol.41, No.3 (2000), 377-380 10.1016/S0040-4039(99)01897-3 00404039 2-s2.0-0034650831 https://repository.li.mahidol.ac.th/handle/123456789/25880 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034650831&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 Tanasri Bunlaksananusorn Patoomratana Tuchinda A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| description |
A convenient and general synthetic method for spiro[4.n]alk-2-ene-1,6- diones and spiro[5.n]alk-2-ene-1,7-diones, which involves the intramolecular acylation of an α-sulfinyl carbanion, is described. |
| author2 |
Mahidol University |
| author_facet |
Mahidol University Manat Pohmakotr Tanasri Bunlaksananusorn Patoomratana Tuchinda |
| format |
Article |
| author |
Manat Pohmakotr Tanasri Bunlaksananusorn Patoomratana Tuchinda |
| author_sort |
Manat Pohmakotr |
| title |
A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| title_short |
A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| title_full |
A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| title_fullStr |
A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| title_full_unstemmed |
A general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| title_sort |
general strategy to spiro[4.n]alk-2-ene-1,6-diones and spiro[5.n]alk- 2-ene-1,7-diones via intramolecular acylation of α-sulfinyl carbanions |
| publishDate |
2018 |
| url |
https://repository.li.mahidol.ac.th/handle/123456789/25880 |
| _version_ |
1763497997064208384 |