One-pot, oxidative and selective conversion of benzylic silyl and tetrahydropyranyl ethers to gem-dichlorides using trichloroisocyanuric acid and triphenylphosphine as an efficient and neutral system
Author:
Affiliation:
1. School of Chemistry, Damghan University, Damghan, Iran
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426507.2020.1845680
Reference31 articles.
1. Synthesis of 2-Keto(hetero)aryl Benzox(thio)azoles through Base Promoted Cyclization of 2-Amino(thio)phenols with α,α-Dihaloketones
2. Stereospecific reductive coupling polymerization of bis(benzylic gem-dibromide)s via formation of a trans-CC bond
3. Carbonyl Olefination by Means of a gem-Dichloride−Cp2Ti[P(OEt)3]2 System
4. Transformation of Aldehydes into (E)-1-Alkenylboronic Esters with a Geminal Dichromium Reagent Derived from a Dichloromethylboronic Ester and CrCl2
5. Organometallic compounds of Group III. Part 43. Alkylenation with geminal dialuminoalkane reagents: the synthesis of olefins from ketones
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