详细信息
Skeletal rearrangement in the Ritter reaction of turpentine: A novel synthesis of p-menthane diamides ( SCI-EXPANDED收录) 被引量:5
文献类型:期刊文献
英文题名:Skeletal rearrangement in the Ritter reaction of turpentine: A novel synthesis of p-menthane diamides
作者:Xu, Shi-Chao[1,2,3,4,5,6] Zhu, Shou-Ji[1,2,3,4] Chen, Yu-Xiang[1,2,3,4,5] Wang, Jing[1,2,3,4,5,6] Bi, Liang-Wu[1,2,3,4,5,6] Lu, Yan-Ju[1,2,3,4,5,6] Gu, Yan[1,2,3,4,5] Zhao, Zhen-Dong[1,2,3,4,5,6]
第一作者:Xu, Shi-Chao;徐士超
通信作者:Xu, SC[1];Xu, SC[2];Xu, SC[3]
机构:[1]Chinese Acad Forestry, Inst Chem Ind Forest Prod, Nanjing 210042, Peoples R China;[2]Key Lab Biomass Energy & Mat, Nanjing 210042, Jiangsu, Peoples R China;[3]Natl Engn Lab Biomass Chem Utilizat, Nanjing 210042, Peoples R China;[4]State Forestry Adm, Key & Open Lab Forest Chem Engn, Nanjing 210042, Peoples R China;[5]Chinese Acad Forestry, Res Inst Forestry New Technol, Beijing 100091, Peoples R China;[6]Jiangxi Agr Univ, 2011 Collaborat Innovat Ctr Jiangxi Typical Tree, Nanchang 330045, Jiangxi, Peoples R China
年份:2017
期号:2
起止页码:124-127
外文期刊名:JOURNAL OF CHEMICAL RESEARCH
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000397134900015),CCR-EXPANDED(收录号:WOS:000397134900015)】;
基金:This project was supported financially by "the National Science Foundation of China (Grant No. 31600466), the Key Projects in the National Science & Technology Pillar Program during the 12th Five-year Plan Period (Grant No. 2015BAD15B04), the Fundamental Research Funds for the Central Non-profit Research Institution of CAF (Grant No. CAFYBB2014QA022), the Fundamental Research Funds for Jiangsu Key Laboratory of Biomass Energy and Materials (Grant No. JSBEM-S-201605) and the National Science Foundation of China (Grant No. 31600466).
语种:英文
外文关键词:Ritter reaction; skeleton rearrangement; synthesis; p-menthane diamides
摘要:A novel skeletal rearrangement in the Ritter reaction was examined which conveniently generated p-menthane diamides from turpentine. A probable reaction mechanism was proposed based on employing thermodynamic analysis. All the products were purified and characterised by H-1 NMR, IR, X-ray crystallography and ESI+-MS.
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