Synthesis of Enantiomerically Pure 1,5,5-Trideuteratedcis- andtrans-2,4-Dioxa-3-phosphadecalins.31P-NMR Evidence of Covalent-Bond Formation and the Stereochemical Implications in the Course of the Inhibition ofδ-Chymotrypsin
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference41 articles.
1. Stereochemistry of the Inhibition of δ-Chymotrypsin with Optically Active Bicyclic Organophosphates:31P-NMR studies
2. Stereochemistry of the Inhibition of δ-Chymotrypsin with Optically Activecis-Decaline-Type Organophosphates:31P-NMR studies
3. 2,4-Dioxa-7-aza-, 2,4-Dioxa-8-aza-, and 2,4-Dioxa-9-aza-3-phosphadecalins as Rigid Acetylcholine Mimetics: Syntheses and Characterization
4. 3-Fluoro-2,4-dioxa-7-aza-3-phosphadecalin 3-Oxides as Rigid Acetylcholine Mimetics: Conformational Analysis and Direct Evidence of the Anomeric Effect
5. Covalent-Bond Formation in the Course of the Inhibition ofδ-Chymotrypsin withtrans-Decalin-Type Organophosphates:31P-NMR Evidence
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4. Synthesis and Characterization of Enantiomerically Pure cis- and trans-3-Fluoro-2,4-dioxa-8-aza-3-phosphadecalin 3-Oxides as γ-Homoacetylcholine Mimetics and Inhibitors of Acetylcholinesterase;Helvetica Chimica Acta;2012-01
5. Synthesis and Characterization of Enantiomerically Pure cis- and trans-3-Fluoro-2,4-dioxa-9-aza-3-phosphadecalin 3-Oxides as Acetylcholine Mimetics and Inhibitors of Acetylcholinesterase;Helvetica Chimica Acta;2011-05
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