2-Chlorotetrafluoroethanesulfinamide induced asymmetric vinylogous Mannich reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference44 articles.
1. Synthesis of enantiomerically pure 2,3-dideoxy-hept-2-enono-1,4-lactone derivatives diastereoselective addition of 2-(trimethylsiloxy)furan to -glyceraldehyde and -serinal-based three-carbon synthons
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3. Furan-, Pyrrole-, and Thiophene-Based Siloxydienes for Syntheses of Densely Functionalized Homochiral Compounds
4. Evolution of the Vinylogous Mannich Reaction as a Key Construction for Alkaloid Synthesis
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2. Synthesis of γ-Lactams via Pd(II)-Catalyzed C(sp3)–H Olefination Using a Self-Cleaving Polyfluoroethylsulfinyl Directing Group;Organic Letters;2020-09-02
3. Synthesis of N–H-Free 1,4-Dihydroisoquinoline-3(2H)-ones via Pd-Catalyzed C–H Olefination Using Polyfluorosulfinyl as the Auxiliary Group;Organic Letters;2020-07-29
4. Diastereoselective vinylogous Mannich reaction of perfluoroalkylated cyclic imines with 2-trimethylsilyloxyfuran;Mendeleev Communications;2019-01
5. Enantioselective Synthesis of Tertiary Trifluoromethyl Carbinols by Vinylogous Aldol Reaction of 3-Methylcyclohex-2-en-1-one with (Het)aryl Trifluoromethyl Ketones;Synlett;2018-12-10
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