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One-Pot and Unsymmetrical Bis-Allylation of Malononitrile with Conjugated Dienes and Allylic Alcohols

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ORGANIC LETTERS
卷 24, 期 51, 页码 9355-9360

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c03405

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资金

  1. National Natural Science Foundation of China
  2. Natural Science Foundation of Jiangsu Province, China
  3. Six Talent Peaks Project in Jiangsu Province
  4. [21702108]
  5. [BK20211257]
  6. [BK20160977]
  7. [YY-033]

向作者/读者索取更多资源

A Pd/Ca catalytic system for the unsymmetrical bis-allylation of malononitrile was developed using conjugated dienes and allylic alcohols as allylic reagents. This system shows high chemoselectivity and efficiency, allowing the synthesis of diverse 1,6-dienes.
A Pd/Ca catalytic system to promote the unsymmetrical bis-allylation of malononitrile was developed by selecting conjugated dienes and allylic alcohols as allylic reagents. This catalytic system suppressed the competitive symmetrical bisallylation process and guaranteed the desired unsymmetrical bisallylation with high chemoselectivity. A wide range of conjugated dienes and allylic alcohols were tolerated well in this transformation, and diverse 1,6-dienes were obtained with high efficiency.

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