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Azobenzene-based unnatural amino acid scaffolds via a Pd(II)-catalyzed C(sp3)–H arylation strategy.
- Source :
- Chemical Communications; 12/4/2022, Vol. 58 Issue 93, p12967-12970, 4p
- Publication Year :
- 2022
-
Abstract
- Azobenzene-based unnatural amino acid motifs were synthesized via Pd(II)-catalyzed diastereoselective C(sp<superscript>3</superscript>)–H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling. [ABSTRACT FROM AUTHOR]
- Subjects :
- ARYLATION
CARBOXAMIDES
Subjects
Details
- Language :
- English
- ISSN :
- 13597345
- Volume :
- 58
- Issue :
- 93
- Database :
- Complementary Index
- Journal :
- Chemical Communications
- Publication Type :
- Academic Journal
- Accession number :
- 160351737
- Full Text :
- https://doi.org/10.1039/d2cc04870a