Golden Opportunities in the Synthesis of Natural Products and Biologically Active Compounds
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John Wiley & Sons, Inc.
Reference129 articles.
1. Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex
2. Asymmetric synthesis of threo- and erythro-sphingosines by asymmetric aldol reaction of α-isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex
3. Application of the gold(I)-Catalyzed aldol reaction to a stereoselective synthesis of (2S, 3R, 4R, 6E)-3-Hydroxy-4-methyl-2-(methylamino)oct-6-enoic Acid ( = MeBmt), Cyclosporin's unusual amino acid
4. Two Chiral Syntheses of threo-3-Hydroxylsine
5. Enantioselective Total Synthesis of (−)-α-Kainic Acid through Free Radical Cyclization of an Alkenyl Monothioformimide
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1. Strategies and Methodologies for the Synthesis of Cyclic Ethers;Methodologies in Ether Synthesis;2024-08-16
2. Total Synthesis of Natural Products using Gold Catalysis;Chemistry – An Asian Journal;2022-11-02
3. Stereoselective Catalytic Synthesis of Alkynylated Phosphaethenes Leading to Activation-Free Gold Catalysis;European Journal of Organic Chemistry;2017-12-08
4. Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (−)-Gabosine H and (−)-6-epi-Gabosine H;Organic Letters;2016-07-26
5. N-Allenyl Amides and O-Allenyl Ethers in Enantioselective Catalysis;European Journal of Organic Chemistry;2016-05-25
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