Synthesis and Mechanistic Study of Fused 2-Pyrrolines via Thermolysis of 6-Substituted-3,5-hexadienyl Azidoformates
Author:
Affiliation:
1. Department of Chemistry, National Cheng Kung University, Tainan, Taiwan 701, Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo010218j
Reference71 articles.
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3. Intramolecular [4 + 1] pyrroline annulation approach to pyrrolizidine alkaloids. Formal total synthesis of (±)-supinidine.
4. The synthesis of pyrrolizidines and indolizidines by the intramolecular cycloaddition of azides with electron-rich 1,3-dienes. A synthetic equivalent of a nitrene-diene cycloaddition
5. Synthesis of fused pyrrolines by the intramolecular cycloadition of azides application to the pyrrolizidine alkaloids.
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2. Stereoselective Synthesis of Pyrido- and Pyrrolo[1,2-c][1,3]oxazin-1-ones via a Nucleophilic Addition–Cyclization Process of N,O-Acetal with Ynamides;The Journal of Organic Chemistry;2018-12-21
3. Substrate scope and stereocontrol in the Rh(II)-catalysed oxyamination of allylic carbamates;Tetrahedron;2014-10
4. Remote Functionalization of C60 with Enantiomerically Pure cyclo-[2]-Malonate Tethers Bearing C12 and C14 Spacers: Synthetic Access to Bisadducts of C60 with the Inherently Chiral trans-3 Addition Pattern;The Journal of Organic Chemistry;2013-07-17
5. An Efficient, Overall [4+1] Cycloadditon of 1,3-Dienes and Nitrene Precursors;Chemistry - A European Journal;2011-09-02
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