A novel stereoselective route to γ-butyrolactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. A general and concise stereodivergent chiral pool approach toward trans-(4S,5R)- and cis-(4R,5R)-5-alkyl-4-methyl-γ-butyrolactones: Syntheses of (+)-trans- and (+)-cis-whisky and cognac lactones from d-(+)-mannitol;Carbohydrate Research;2021-12
2. Lactone and Lactam Formation;Comprehensive Organic Transformations;2018-02-28
3. Reactions of organoboranes with carbanions bearing three potential leaving groups: unusual processes, products and mechanisms;Tetrahedron;2016-11
4. Alkyne-Mediated Approach to the Synthesis of (4R,5R)-5-Hydroxy-4-decanolide and (−)-Muricatacin;Helvetica Chimica Acta;2015-07
5. Naturally Occurring Limonene to Cinnamyl-type γ-Butyrolactone Substituted Aldol Condensation Derivatives as Antioxidant Compounds;Natural Product Communications;2012-09
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