Sharma, Pallavi, Moorhouse, Adam D, Moses, John E (October 2011) Microwave-Enhanced Reaction of Thioacids with Azides in Aqueous Medium. Synlett: accounts and rapid communications in synthetic organic chemistry, 2011 (16). pp. 2384-2386. ISSN 0936-5214
Abstract
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. Starting from substituted anilines, in situ formation of the corresponding aromatic azide is followed by their immediate reaction with a thioacid to yield amides in excellent yield. This improved protocol significantly reduces the reaction time thus increasing the overall efficiency of this useful transformation. © Georg Thieme Verlag Stuttgart - New York.
| Item Type: | Paper |
|---|---|
| Subjects: | chemistry > chemicals > aromatic azides chemistry > techniques > click chemistry chemistry > techniques > microwaves chemistry > chemicals > thio acids |
| CSHL Authors: | |
| SWORD Depositor: | CSHL Elements |
| Depositing User: | CSHL Elements |
| Date: | October 2011 |
| Date Deposited: | 02 Jul 2021 14:21 |
| Last Modified: | 02 Jul 2021 14:21 |
| Related URLs: | |
| URI: | https://repository.cshl.edu/id/eprint/40242 |
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