Direct Synthesis of Enolizable  N ‐Sulfonyl Ketimines Under Microwave Irradiation | Zendy

Collados Juan F. | Zendy; Harutyunyan Syuzanna R. | Zendy

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Direct Synthesis of Enolizable N ‐Sulfonyl Ketimines Under Microwave Irradiation

Author(s) -

Collados Juan F.,

Harutyunyan Syuzanna R.

Publication year - 2016

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201600022

Subject(s) - sulfonyl , chemistry , sulfonamide , microwave irradiation , aldimine , aldehyde , microwave , combinatorial chemistry , organic chemistry , condensation , catalysis , alkyl , physics , quantum mechanics , thermodynamics

N ‐sulfonyl imines are widely used as substrates for a range of transformations. Access to N ‐sulfonyl aldimines is straightforward through direct condensation between the parent aldehyde and the sulfonamide. However, this approach is not efficient for the synthesis of enolizable N ‐sulfonyl ketimines. Herein we report a rapid and facile methodology for obtaining these products using microwave irradiation.

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