One Pot Photoredox  Decarboxylation  Reaction of  N ‐Cyano(α‐bromo‐α‐phenyl)methylanilines Leading to Synthesis of Four‐Membered Cyclic Carbamates | Zendy

Kaur Manpreet | Zendy; Singh Baldev | Zendy

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One Pot Photoredox Decarboxylation Reaction of N ‐Cyano(α‐bromo‐α‐phenyl)methylanilines Leading to Synthesis of Four‐Membered Cyclic Carbamates

Author(s) -

Kaur Manpreet,

Singh Baldev

Publication year - 2014

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.1776

Subject(s) - chemistry , decarboxylation , salt (chemistry) , proton nmr , iodide , elemental analysis , medicinal chemistry , aqueous medium , carbon 13 nmr , aqueous solution , organic chemistry , catalysis

A new four‐membered cyclic carbamates have been synthesized through solar irradiation of N ‐cyano(α‐bromo‐α‐phenyl)methylanilines in their aqueous methanolic solution using iodide salt in basic medium. These compounds have been characterized as 3,4‐diphenyl‐1,3oxazetidin‐2‐one through their elemental analysis, IR, 1 H‐NMR, 13 C‐NMR, and mass spectral studies.

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