One-pot two-step reaction of selenosulfonate with isocyanides and allyl alcohol under aqueous conditions: Atom-economic synthesis of selenocarbamates and allyl sulfones-Reference-Cited by-同舟云学术

One-pot two-step reaction of selenosulfonate with isocyanides and allyl alcohol under aqueous conditions: Atom-economic synthesis of selenocarbamates and allyl sulfones

Published:2021-02 Issue:2 Volume:32 Page:721-724
ISSN:1001-8417
Container-title:Chinese Chemical Letters
language:en
Short-container-title:Chinese Chemical Letters

Author:

Ai Jing-Jing,Li Jian,Ji Shun-Jun^ORCID,Wang Shun-Yi^ORCID

Funder

National Natural Science Foundation of China

Ph.D. Programs Foundation of PAPD

Project of Scientific and Technologic Infrastructure of Suzhou

Major Basic Research Project of the Natural Science Foundation of the Jiangsu Higher Education Institutions

Soochow University, and State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials

Publisher

Elsevier BV

Subject

General Chemistry

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1. Organoselenium and Organotellurium Compounds: Toxicology and Pharmacology

2. Ligand-Controlled Regioselectivity in the Hydrothiolation of Alkynes by Rhodium N-Heterocyclic Carbene Catalysts

3. Trifluoromethanesulfanylamides as Easy-to-Handle Equivalents of the Trifluoromethanesulfanyl Cation (CF3S+): Reaction with Alkenes and Alkynes

4. Sandmeyer trifluoromethylthiolation of arenediazonium salts with sodium thiocyanate and Ruppert–Prakash reagent

5. Nickel-Catalyzed Synthesis of Aryl Trifluoromethyl Sulfides at Room Temperature

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