110166-75-1Relevant articles and documents
Oxypalladation Initiating the Oxid-ative Heck Reaction with Alkenyl -Alcohols: Synthesis of Isocoumarin–Alkanones
Zheng, Meifang,Huang, Liangbin,Tong, Qizhen,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 663 - 667 (2017/01/18)
Highly regioselective nucleopalladation for the oxidative coupling of internal alkynes with alkenyl alcohols by using green and low-costing oxygen as the sole oxidant was investigated. This one-pot cascade cyclization proceeds through Pd-catalyzed intramolecular C–O bond cyclization, insertion of nonbiased alkenyl alcohols, β-H elimination, and reinsertion of a HPdX species, which is finally transferred to the target ketones. This method has the advantages of mild conditions, good functional group tolerance, and can be performed with unactivated alkenes to afford isocoumarin derivatives.
Condensed heteroaromatic ring systems. VIII. Synthesis of 3-substituted isocoumarins from o-halobenzoic acid derivatives
Sakamoto,An-naka,Kondo,Yamanaka
, p. 2754 - 2759 (2007/10/02)
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