Asymmetric synthesis of 3-alkyl substituted prolines by alkylation of a chiral sulfone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Regioselective Enolization and Alkylation of 4-Oxo-N-(9-phenylfluoren-9-yl)proline: Synthesis of Enantiopure Proline−Valine and Hydroxyproline−Valine Chimeras
2. A Novel Stereodivergent Synthesis of Optically Pure cis- and trans-3-Substituted Proline Derivatives
3. trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyl-L-proline derivatives from 4-hydroxy-L-proline
4. 2,3-Substituted 2-azanorbornanes as polar β-turn mimetics
5. Further Delineation of the Two Binding Sites (R*n) Associated with Tachykinin Neurokinin-1 Receptors Using [3-Prolinomethionine11]SP Analogues
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1. Asymmetric sulfonylation with sulfur dioxide surrogates: a new access to enantiomerically enriched sulfones;Chemical Communications;2023
2. Advances in Synthesis of Enantioenriched Chiral Sulfones by Enantioselective Conjugate Addition Reactions;Asian Journal of Organic Chemistry;2021-12-06
3. Carbozincation Reactions of Carbon-Carbon Multiple Bonds;Organic Reactions;2015-09-18
4. Organocatalytic Michael Addition of Nitro Esters to α,β-Unsaturated Aldehydes: Towards the Enantioselective Synthesis oftrans-3-Substituted Proline Derivatives;Advanced Synthesis & Catalysis;2012-09-03
5. Catalytic Asymmetric Synthesis of 3-Substituted Proline Derivatives by Using Phase-Transfer-Catalyzed Conjugate Addition;Asian Journal of Organic Chemistry;2012-07-29
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