Chamuah, Ajay and D S, Sharada
(2016)
An Access to Fully Substituted β-Iodo N-Arylated Enamines via Dehydrogenative Iodoarylation of Vinylogous Carbamates Using Phenyliodine(III)diacetate(PIDA).
Masters thesis, Indian Institute of Technology Hyderabad.
Abstract
A novel and facile dehydrogenative iodoarylation of N-aryl vinylogous carbamates with hypervalent iodine (III) as
the source of aryl and iodide has been developed. This protocol provides a valuable synthetic tool for the assembly of a wide range of β-iodo N-arylated enamines under mild conditions with functional group tolerance and scalability. This attractive route for the synthesis of β-iodo N-arylated enamines is of great importance due to the product versatile reactivity for further transformations.
[error in script]
| IITH Creators: |
| IITH Creators | ORCiD |
|---|
| D S, Sharada | UNSPECIFIED |
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| Item Type: |
Thesis
(Masters)
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| Uncontrolled Keywords: |
organic synthesis, N-aryl vinylogous carbamates, scalability, TD504 |
| Subjects: |
?? sub5.8 ?? |
| Divisions: |
Department of Chemistry |
| Depositing User: |
Library Staff
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| Date Deposited: |
05 May 2016 05:08 |
| Last Modified: |
22 May 2019 04:03 |
| URI: |
http://raiithold.iith.ac.in/id/eprint/2317 |
| Publisher URL: |
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| Related URLs: |
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