P(NMe 2 ) 3 ‐Mediated Reductive (1+4) Annulation Reaction of α ‐Keto Esters with Nitroalkenes: A Facile Synthesis of Polysubstituted Isoxazoline N ‐Oxides
Author:
Affiliation:
1. State Grid Hunan Electric Power Corporation Limited Research Institute Changsha 410007 P.R. China
2. The State Key Laboratory of Elemento-Organic Chemistry and College of Chemistry Nankai University Tianjin 100193 P.R. China
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202004503
Reference60 articles.
1. Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems
2. For selected examples see:
3. A novel palladium-catalyzed cycloalkylation to isoxazoline 2-oxides. Application for the asymmetric synthesis of carbanucleosides.
4. Total synthesis of calicheamicin .gamma.1I. 2. Development of an enantioselective route to (-)-calicheamicinone
5. Silicon-Tethered 1,3-Dipolar Cycloaddition of 4-Hydroxy-2-isoxazoline 2-Oxides
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1. Sequential In Situ-Formed Kukhtin–Ramirez Adduct and P(NMe2)3-Catalyzed O-Phosphination of α-Dicarbonyls with P(O)–H;Organic Letters;2023-10-13
2. P(NMe 2 ) 3 ‐Mediated Reductive (1+4) Annulation Reaction of α ‐Keto Esters with Nitroalkenes: A Facile Synthesis of Polysubstituted Isoxazoline N ‐Oxides;ChemistrySelect;2021-05-05
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