Application of the asymmetric Diels–Alder reaction of a 2-substituted chiral maleate to the formal synthesis of (−)-β-santalene
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference15 articles.
1. Total Syntheses, Optical Rotations and Fragrance Properties of Sandalwood Constituents: (−)-(Z)- and (−)-(E)-β-Santalol and Their Enantiomers,ent-β-Santalene
2. AsymmetricDiels-Alder Reactions of Neopentyl-Ether-Shielded Acrylates and Allenic Esters: Syntheses of (?)-Norbornenone and (?)-?-Santalene
3. Enantiodivergent route to both enantiomers of β-santalene and epi-β-santalene from a single chiral template
4. The Asymmetric Diels–Alder Cycloaddition Using Ethyl (−)-(Z)-(R)S-2-Methyl-3-(p-tolylsulfinyl)propenoate: Application to an Enantioselective Synthesis of (+)-epi-β-Santalene
5. Asymmetric Diels-Alder and Ene Reactions in Organic Synthesis. New Synthetic Methods(48)
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1. Omics in Sandalwood;Materials Horizons: From Nature to Nanomaterials;2022
2. The Synthesis of Fragrant Natural Products from Santalum album L.: (+)-(Z)-?-Santalol and (–)-(Z)-?-Santalol;CHIMIA;2017-12-01
3. Synthesis of a Functionalized 7,6-Bicyclic Spiroimine Ring Fragment of the Spirolides;Organic Letters;2010-10-28
4. Enantioselective Synthesis of (−)-β-Santalol by a Copper-Catalyzed Enynol Cyclization-Fragmentation Reaction;Angewandte Chemie International Edition;2009-09-14
5. Enantioselective Synthesis of (−)-β-Santalol by a Copper-Catalyzed Enynol Cyclization-Fragmentation Reaction;Angewandte Chemie;2009-09-14
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