Aminoisocyanides in Multicomponent Reactions (MCRs): A Facile Synthesis of Substituted 3(5H)-Pyrrolin-2-ones via a Dimroth-type Rearrangement
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-07-05
著者
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NAIR Vijay
Organic Chemistry Division, Regional Research Laboratory (CSIR)
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Vinod A.
Organic Chemistry Division Regional Research Laboratory (csir)
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Nair Vijay
Organic Chemistry Division Regional Research Laboratory (csir)
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MATHEN Joseph
Organic Chemistry Division, Regional Research Laboratory (CSIR)
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VARMA R.
Organic Chemistry Division, Regional Research Laboratory (CSIR)
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Mathen Joseph
Organic Chemistry Division Regional Research Laboratory (csir)
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Varma R.
Organic Chemistry Division Regional Research Laboratory (csir)
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- Aminoisocyanides in Multicomponent Reactions (MCRs): A Facile Synthesis of Substituted 3(5H)-Pyrrolin-2-ones via a Dimroth-type Rearrangement
- Dipolar Cycloaddition Reactions of Isatin Derived Azomethine Ylide with 3, 4-Diphenylcyclobutene-1, 2-dione:Synthesis of Novel Spiro[oxidole-3, 2'-pyrrolidine]Derivatives
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