Stereoselective synthesis of the obscure mealybug pheromone by hydrogenation of a tetrasubstituted alkene precursor
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. (2,3,4,4-Tetramethylcyclopentyl)Methyl Acetate, a Sex Pheromone from the Obscure Mealybug: First Example of a New Structural Class of Monoterpenes
2. IPM pest management guidelines grape, insects and mites;Bentley,2004
3. Synthesis of the sex pheromone of the obscure mealybug, the first example of a new class of monoterpenoids
4. Determination of the absolute configuration of the sex pheromone of the obscure mealybug by vibrational circular dichroism analysis
5. Enantioselective Synthesis of a Mealybug Pheromone with an Irregular Monoterpenoid Skeleton
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2. Large-Scale Enantioselective Reduction of 2,3-Disubstituted Indenopyridine Enables a Practical Manufacturing Process for an 11β-HSD-1 Inhibitor;Organic Process Research & Development;2021-11-08
3. Stereoselective Synthesis of Tetrasubstituted Alkenes via a Cp*Co III ‐Catalyzed C−H Alkenylation/Directing Group Migration Sequence;Angewandte Chemie International Edition;2017-05-16
4. Stereoselective Synthesis of Tetrasubstituted Alkenes via a Cp*Co III ‐Catalyzed C−H Alkenylation/Directing Group Migration Sequence;Angewandte Chemie;2017-05-16
5. Semiochemicals in Mealybugs;Mealybugs and their Management in Agricultural and Horticultural crops;2016
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