An article Catalytic, Asymmetric Dearomative Synthesis of Complex Cyclohexanes via a Highly Regio- and Stereoselective Arene Cyclopropanation Using alpha-Cyanodiazoacetates WOS:000526394200001 published article about INTRAMOLECULAR BUCHNER REACTION; ENANTIOSELECTIVE EPOXIDATION; DIAZO-COMPOUNDS; EPOXIDES; ACID; REARRANGEMENT; DIHYDROXYLATION; SELECTIVITY; OXIDATION; SYSTEMS in [Smith, Kendrick L.; Padgett, Cody L.; Mackay, William D.; Johnson, Jeffrey S.] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA in 2020.0, Cited 79.0. Product Details of 95-49-8. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8
Arene cyclopropanation offers a direct route to higher-order, non-aromatic carbocycles; however, the inherent issue of dictating site selectivity has cumbered the development of novel intermolecular reactions that directly engage the arene pool. This paper describes a highly regio- and stereoselective, Rh-2[(S)-PTTL](4)-catalyzed arene cyclopropanation using alpha-cyanodiazoacetates to afford stable norcaradienes bearing three stereogenic centers, one of which is an all-carbon quaternary center. The enantioenriched norcaradienes served as tunable templates for further transformation into stereochemically dense, fused and bicyclic carbocycles containing transmutable functionality.
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Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
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