Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. A molecular electron density theory study of asymmetric Diels–Alder [4 + 2] reaction’s mechanism of furan with three substituted alkynes (5-R substituted-3-(3-(phenylsulfonyl)-propioloyl)-oxazolidin-2-one);Journal of Molecular Modeling;2023-08-23
2. Noncovalent Interactions in the Oxazaborolidine-Catalyzed Enantioselective Mukaiyama Aldol;The Journal of Organic Chemistry;2022-07-18
3. Asymmetric Diels–Alder reaction between furans and propiolates;Tetrahedron Letters;2021-05
4. Enamides and dienamides in phosphoric acid-catalysed enantioselective cycloadditions for the synthesis of chiral amines;Chemical Communications;2021
5. Applications of Diels–Alder cycloaddition reaction in total synthesis of alkaloids;Recent Applications of Selected Name Reactions in the Total Synthesis of Alkaloids;2021
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