First N-alkyl heterolysis of tertiary benzamides in neutral conditions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Brown, R. S.; Bennet, A. J.; Slebocka-Tilk, H. Acc. Chem. Res. 1992, 11, 481–488 and references cited therein.
2. Distorted amides as models for activated peptide N-C(O) units. 3. Synthesis, hydrolytic profile, and molecular structure of 2,3,4,5-tetrahydro-2-oxo-1,5-propanobenzazepine
3. Structures and energetics of two bridgehead lactams and their N- and O-protonated forms: an ab initio molecular orbital study
4. N-Protonation vs O-Protonation in Strained Amides: Ab Initio Study
5. Distorted amides as models for activated peptide N-C:O units produced during enzyme-catalyzed acyl transfer reactions. 1. The mechanism of hydrolysis of 3,4-dihydro-2-oxo-1,4-ethanoquinoline and 2,3,4,5-tetrahydro-2-oxo-1,5-ethanobenzazepine
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2. Asymmetric synthesis of 2H-aziridine phosphonates, and α- or β-aminophosphonates from enantiomerically enriched 2H-azirines;Tetrahedron: Asymmetry;2003-03
3. Incorporation of Ahc into Model Dipeptides as an Inducer of a β-Turn with a Distorted Amide Bond. Conformational Analysis;The Journal of Organic Chemistry;2002-05-17
4. ChemInform Abstract: First N-Alkyl Heterolysis of Tertiary Benzamides in Neutral Conditions.;ChemInform;2001-02-27
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