4.7 Article

An Unexpected Domino Reaction of β-Keto Sulfones with Acetylene Ketones Promoted by Base: Facile Synthesis of 3(2H)-Furanones and Sulfonylbenzenes

期刊

ADVANCED SYNTHESIS & CATALYSIS
卷 359, 期 22, 页码 4025-4035

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201700830

关键词

acetylene ketones; domino reaction; -keto sulfones; reaction regioselectivity; sulfonylbenzenes

资金

  1. National Natural Science Foundation of China [21362002, 81260472]
  2. Guangxi Natural Science Foundation of China [2014GXNSFDA118007, 2016GXNSFEA380009, 2016GXNSFGA380005]
  3. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2014A02, CMEMR2012A20]
  4. Guangxi's Medicine Talented Persons Small Highland Foundation [1306]
  5. Youth Promotion Project Fund of Guangxi [30606017004]

向作者/读者索取更多资源

An unexpected domino reaction of beta-keto sulfones with acetylene ketones has been developed. The domino reaction of beta-keto sulfones with diynones proceeded smoothly in the presence of 30mol% K2CO3 without other additives, and afforded the novel 3(2H)-furanone derivatives. On replacing the diynones with terminal alkyne ketones, the reaction regioselectivity was changed and sulfonylbenzenes were obtained via benzannulation in good yields.

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