中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Metal-Free 1,8-Diazabicyclo(5.4.0)-undec-7-ene Mediated Synthesis of α-Acetal Amides through Reaction of Glyoxylic Acid Acetalde with Aryl Isothiocyanates

文献类型:期刊论文

作者Ding Rou; Shi Siyu; Ma Chao; Wei Wei; Lu Yufen
刊名CHINESE JOURNAL OF ORGANIC CHEMISTRY
出版日期2024
卷号44期号:7
英文摘要Metal-free condensation reaction of glyoxylic acid acetalde with aryl isothiocyanates leading to alpha-acetal amides has been reported. The present protocol, which simply utilizes 1,8-diazabicyclo(5.4.0)-undec-7-ene (DBU) as base, provides a green and efficient approach to construct a series of alpha-acetal amides in the absence of metal catalysts and stoichiometric amounts of coupling reagents.
源URL[http://210.75.249.4/handle/363003/61997]  
专题西北高原生物研究所_中国科学院西北高原生物研究所
推荐引用方式
GB/T 7714
Ding Rou,Shi Siyu,Ma Chao,et al. Metal-Free 1,8-Diazabicyclo(5.4.0)-undec-7-ene Mediated Synthesis of α-Acetal Amides through Reaction of Glyoxylic Acid Acetalde with Aryl Isothiocyanates[J]. CHINESE JOURNAL OF ORGANIC CHEMISTRY,2024,44(7).
APA Ding Rou,Shi Siyu,Ma Chao,Wei Wei,&Lu Yufen.(2024).Metal-Free 1,8-Diazabicyclo(5.4.0)-undec-7-ene Mediated Synthesis of α-Acetal Amides through Reaction of Glyoxylic Acid Acetalde with Aryl Isothiocyanates.CHINESE JOURNAL OF ORGANIC CHEMISTRY,44(7).
MLA Ding Rou,et al."Metal-Free 1,8-Diazabicyclo(5.4.0)-undec-7-ene Mediated Synthesis of α-Acetal Amides through Reaction of Glyoxylic Acid Acetalde with Aryl Isothiocyanates".CHINESE JOURNAL OF ORGANIC CHEMISTRY 44.7(2024).

入库方式: OAI收割

来源:西北高原生物研究所

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