Metal-Free Oxidative Nitration of α-Carbon of Carbonyls Leads to One-Pot Synthesis of Thiohydroximic Acids from Acetophenones-Reference-Cited by-同舟云学术

Metal-Free Oxidative Nitration of α-Carbon of Carbonyls Leads to One-Pot Synthesis of Thiohydroximic Acids from Acetophenones

Published:2016-08-19 Issue:17 Volume:18 Page:4190-4193
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dighe Shashikant U.¹,Mukhopadhyay Sushobhan¹,Priyanka Kumari¹,Batra Sanjay¹²

Affiliation:

1. Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India

2. Academy of Scientific and Innovative Research, New Delhi 110025, India

Funder

Central Drug Research Institute

Council for Scientific and Industrial Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01807

Reference52 articles.

1. Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cycloetherification

2. In Situ Generated (Hypo)Iodite Catalysts for the Direct α-Oxyacylation of Carbonyl Compounds with Carboxylic Acids

3. High-turnover hypoiodite catalysis for asymmetric synthesis of tocopherols

4. Chiral Ammonium Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of 1-Naphthols Using Hydrogen Peroxide

5. Chiral Ammonium Hypoiodite Salt-catalyzed Enantioselective Oxidative Cycloetherification to 2-Acyl Tetrahydrofurans

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