An asymmetric dihydroxylation route to (−)-bulgecinine
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference36 articles.
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1. A glycal based approach to the synthesis of (+)-bulgecinine, 3-hydroxy-2,5-dihydroxymethylpyrrolidine and 2-oxapyrrolizidin-3-one;Carbohydrate Research;2020-03
2. Synthesis of (–)-Bulgecinine and 5-epi-Bulgecinine through Proline-Catalysed Asymmetric α-Hydroxylation of an Aldehyde Derived from l-Glutamic Acid;SynOpen;2019-10
3. Direct Reductive Cyanation of A 2-Pyrrolidinone Chiral Building Block Bearing An Unprotected Hydroxyl Group: A Stereoselective Synthesis of N-Methyl-2-epi-bulgecinine;Chinese Journal of Organic Chemistry;2017
4. Development of Stereoselective Synthesis of Biologically Active Nitrogen-heterocyclic Compounds: Applications for Syntheses of Natural Product and Organocatalyst;Journal of Synthetic Organic Chemistry, Japan;2016
5. Catalyst design in oxidation chemistry; from KMnO4 to artificial metalloenzymes;Bioorganic & Medicinal Chemistry;2014-10
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