Oxygen-18 scrambling studies in the solvolysis of benzyl tosylates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. The Solvolysis of Benzyl Tosylates. V. Some Solvent Effects
2. New insights into aliphatic nucleophilic substitution reactions from the use of pyridines as leaving groups
3. Substitution at a saturated carbon atom. X. Unification of mechanisms Snl and Sn2
4. Substitution at a saturated carbon atom. XVII. Organic ion pairs as intermediates in nucleophilic substitution and elimination reactions
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2. Reactions of Nitrogen Derivatives of Carbonyl Compounds with Phenyliodoso Diacetate in Organic Synthesis;Current Organic Synthesis;2010-02-01
3. Dynamics for reactions of ion pairs in aqueous solution: reactivity of tosylate anion ion paired with the highly destabilized 1-(4-methylphenyl)-2,2,2-trifluoroethyl carbocation;Journal of Physical Organic Chemistry;2010-01-13
4. Probing the Mechanism of Sulfoxide-Catalyzed Hemiacetal Activation in Dehydrative Glycosylation;The Journal of Organic Chemistry;2005-04-20
5. Reactions of ion-pair intermediates of solvolysis;The Chemical Record;2005
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