Highly stereoselective Friedel–Crafts alkylations of unactivated benzenes by episulfonium ion cyclizations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Enantioselectivity in the ritter-type substitution reaction via qpisulfonium ion: Retention of configuration
2. Retention of configuration in the ritter-type substitution reaction of chiral β-arylthio alcohols through the anchimeric assistance of the arylthio group
3. Preparation of chiral aziridines from chiral oxiranes with retention of configuration
4. Conversion of chiral oxiranes into chiral aziridines with retention of configuration by way of chiral episulfonium ions and reactions of the aziridines with Grignard reagents
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1. Carbosulfenylation of Alkenes with Organozinc Reagents and Dimethyl(methylthio)sulfonium Trifluoromethanesulfonate;Organic Letters;2020-11-30
2. Dehydroxylated C-3 Alkylation of Indole Accompanied by 1,2-Sulfur Migration;The Journal of Organic Chemistry;2020-04-13
3. Stereoselective Haliranium, Thiiranium and Seleniranium Ion‐Triggered Friedel–Crafts‐Type Alkylations for Polyene Cyclizations;Advanced Synthesis & Catalysis;2019-06-26
4. FeCl3-Catalyzed Regio-Divergent Carbosulfenylation of Unactivated Alkenes: Construction of a Medium-Sized Ring;The Journal of Organic Chemistry;2018-08-16
5. Schweinfurthins A–Q: isolation, synthesis, and biochemical properties;RSC Advances;2018
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