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- Organic Letters | Vol 20, Issue 19, Pages 5985-6322 (2018 . . .
Selective Oxidative Dearomatization of Angular Tetracyclic Phenols by Controlled Irradiation under Air: Synthesis of an Angucyclinone-Type Double Peroxide with Anticancer Properties
- I2-Mediated Oxidative C–N and N–S Bond Formation in Water: A . . .
An environmentally benign and convenient strategy for the synthesis of 4,5-disubstituted N-fused 3-amino-1,2,4-triazoles and 3-substituted 5-amino-1,2,4-thiadiazoles from isothiocyanates has been developed This metal-free method involves I 2 -mediated oxidative C–N and N–S bond formations in water
- Oxidative Coupling with S–N Bond Formation - Mulina - 2018 . . .
This is the first exhaustive review relating to achievements in oxidative transformations involving S–N bond formation It summarizes 134 references, mainly from 2000 to 2018, and is divided into chapters according to the classes of compounds synthesized
- Organic Letters Vol. 20 No. 20 - ACS Publications
A synthetic strategy conceived with the intent of establishing a novel approach to the de novo construction of ryanoids is described that is based on a recently developed metallacycle-mediated intramolecular oxidative alkyne–1,3-diketone coupling reaction
- Green Cross-Coupling Using Visible Light for C–O and C–N Bond . . .
Recently, visible-light-mediated photocatalysis has achieved great progress and been a powerful tool to the construction of new chemical bonds in the green synthetic community This chapter provides an updated summary of visible-light-mediated cross-coupling for C–O and C–N bond formations
- Organic Letters | Vol 20, Issue 17, Pages 5082-5527 (2018 . . .
Development of N‑Doped Carbon-Supported Cobalt Copper Bimetallic Nanoparticle Catalysts for Aerobic Oxidative Esterifications Based on Polymer Incarceration Methods
- Photo-induced oxidant-free oxidative C–H N–H cross-coupling . . .
Herein we show a selective C (sp 2)-H amination of arenes (alkyl-substituted benzenes, biphenyl and anisole derivatives) accompanied by hydrogen evolution by using heterocyclic azoles as nitrogen
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