Leaving group, steric and substituent effects in highly congested systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference47 articles.
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3. Solvent effects in the solvolysis of aryldi-tert-butylcarbinyl-p-nitrobenzoates in aqueous acetic acid. Substituent effects on transition state charge separation
4. Steric effects in highly congested systems. Steric retardation in the acid catalysed dehydration of alkyl-di-t-butylcarbinols in anhydrous acetic acid : Comparison with p-nitrobenzoate solvolysis.
5. The importance of leaving group steric effects in solvolysis of tertiary carbinyl systems. Empirical force field treatment of acid-catalyzed dehydration of 2-alkyl-2-adamantanols
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1. Products from the addition of acetoacetic ester or acetylacetone to 3-nitro-2Н-chromenes – axially chiral trans,trans-2,3,4-trisubstituted chromans and related pyrazoles;Chemistry of Heterocyclic Compounds;2015-08
2. Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2Н-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers;Chemistry of Heterocyclic Compounds;2015-06
3. Recent Advances in Atropisomerism;Topics in Stereochemistry;2007-02-26
4. Solvent effects on hydrogen bonding and rotation barriers in α-alkyl-substituted 2-alkoxybenzyl alcohols †;Journal of the Chemical Society, Perkin Transactions 2;2001
5. Computational Measurement of Steric Effects: the Size of Organic Substituents Computed by Ligand Repulsive Energies;The Journal of Organic Chemistry;1999-09-30
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