On-Demand Generation and Use in Continuous Synthesis of the Ambiphilic Nitrogen Source Chloramine-Reference-Cited by-同舟云学术

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On-Demand Generation and Use in Continuous Synthesis of the Ambiphilic Nitrogen Source Chloramine

Published:2020-10-21 Issue:21 Volume:22 Page:8392-8395
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Danahy Kelley E.¹,Styduhar Evan D.¹,Fodness Aria M.¹,Heckman Laurel M.¹,Jamison Timothy F.¹^ORCID

Affiliation:

1. Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 01239, United States

Funder

Defense Advanced Research Projects Agency

Massachusetts Institute of Technology

National Institute of General Medical Sciences

National Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c03021

Reference35 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

2. Direct and Stereospecific Synthesis of N ‐H and N ‐Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine‐ O ‐Sulfonic Acids

3. Sustainable Synthesis of Oximes, Hydrazones, and Thiosemicarbazones under Mild Organocatalyzed Reaction Conditions

4. In Situ Preparation and Consumption of O-Mesitylsulfonylhydroxylamine (MSH) in Continuous Flow for the Amination of Pyridines

5. Reaction scheme for the chlorination of ammoniacal water

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3. A new outlook in oxidative transformations and coupling reactions via in situ generation of organic chloramines;Applied Organometallic Chemistry;2022-01-03

4. Recent advances of aminoazanium salts as amination reagents in organic synthesis;Organic & Biomolecular Chemistry;2022

5. Momentary click nitrile synthesis enabled by an aminoazanium reagent;Organic Chemistry Frontiers;2022

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