32971-17-8Relevant academic research and scientific papers
4,6,8,10,16-Penta- and 4,6,8,10,16,18-Hexamethyldocosanes from the Cane Beetle Antitrogus parvulus - Cuticular Hydrocarbons with Unprecedented Structure and Stereochemistry
Fletcher, Mary T.,Chow, Sharon,Lambert, Lynette K.,Gallagher, Oliver P.,Cribb, Bronwen W.,Allsopp, Peter G.,Moore, Christopher J.,Kitching, William
, p. 5083 - 5086 (2003)
(Equation presented) The major cuticular hydrocarbons from the cane beetle species Antitrogus parvulus were deduced to be 4,6,8,10,16,18-hexa- and 4,6,8,10,16-pentamethyldocosanes 2 and 3, respectively. Isomers of 2,4,6,8-tetramethylundecanal 27, 36, and
Total synthesis of (±)-cordypyridones A and B and related epimers
Jones, Ian L.,Moore, Felicity K.,Chai, Christina L. L.
, p. 5526 - 5529 (2009)
"Chemical Equation Presented" Efficient racemic synthesis of two antibacterial and antimalarial natural products, cordypyridones A and B, was achieved from inexpensive, commercially available starting materials In an overall yield of 15% (8% and 7%, respe
Highly Selective Hydrogenation of Aromatic Ketones and Phenols Enabled by Cyclic (Amino)(alkyl)carbene Rhodium Complexes
Wei, Yu,Rao, Bin,Cong, Xuefeng,Zeng, Xiaoming
supporting information, p. 9250 - 9253 (2015/08/11)
Air-stable Rh complexes ligated by strongly σ-donating cyclic (amino)(alkyl)carbenes (CAACs) show unique catalytic activity for the selective hydrogenation of aromatic ketones and phenols by reducing the aryl groups. The use of CAAC ligands is essential for achieving high selectivity and conversion. This method is characterized by its good compatibility with unsaturated ketones, esters, carboxylic acids, amides, and amino acids and is scalable without detriment to its efficiency.
STEREOCHEMISTRY OF LARDOLURE. THE AGGREGATION PHEROMONE OF THE ACARID MITE, LARDOGLYPHUS KONOI
Mori, Kenji,Kuwahara, Shigefumi
, p. 5545 - 5550 (2007/10/02)
(1R,3R,5R,7R)-Stereochemistry was assigned to lardolure (1,3,5,7-tetramethyldecyl formate) on the basis of GLC comparison of the natural pheromone with the synthetic pheromones prepared in partially stereocontrolled manners.
