John P. Price of 3-Chloro-1H-pyrazole Wolfe of the University of Michigan constructed the cyclobutene 3 by coupling the enol triflate 1 with diethyl malonate 2 (Org. Lett. 2022, 24, 8208.…
Masato Matsugi of Meijo University prepared the carbamoyl azide 2 by reaction of the hydroxamic acid 1 with diphenyl phosphorazidate (Tetrahedron Lett. PMID:32261617 2022, 95, 153727. DOI: 10.1016/j.tetlet.2022.153727). Yan Zhao…
Benjamin Darses of the Université Grenoble-Alpes and Marie Sircoglou and Philippe Dauban of the Université Paris-Saclay effected the enantioselective aziridination of the terminal alkene 1 with 2, leading to 3…
Hongjian Lu of Nanjing University used an Ir catalyst to mediate the regioselective ortho amination of the benzamide 1, leading to the protected anthranilamide 2 (J. Org. 574007-66-2 structure Chem.…
α-Tocopherol Pinhong Chen and Guosheng Liu of the Shanghai Institute of Organic Chemistry developed a protocol for the enantioselective conversion of a terminal alkene 1 to the secondary benzoate 2…
Carbocyclic rings, unlike saturated heterocyclic rings, are not susceptible to the hepatic activation that is the basis of much drug toxicity. To pave the way for pharmaceutical discovery based on…
Oleg V. Larionov of the University of Texas at San Antonio devised a protocol for the decarboxylative coupling of an acid 1 with an arenesulfinate 2 to give the sulfoxide…
Christopher Uyeda of Purdue University achieved high enantioselectivity in the cyclopropanation of myrcene (1) with 2,2-dichloropropane (2) to give 3 (J. Am. Chem. Soc. 2023, 145, 9441. DOI: 10.1021/jacs.3c01949). Qinglei…
Malte Brasholz of the University of Rostock developed a protocol for the photochemically-driven in situ oxidation of the quinoxalinone 1 followed by cycloaddition with methacrylonitrile 2 to give the azetidine…
Vicente Gotor-Fernández and Iván Lavandera of the Universidad de Oviedo optimized the enzymatic reduction of the chloroketone 1 to the chlorohydrin 2, then telescoped that to begin with the 1-chloroalkyne…
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