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Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted alpha-hydroxy-beta-amino amides
Lin, CY (Lin, Chao-Yang); Ma, PJ (Ma, Peng-Ju); Sun, Z (Sun, Zhao); Lu, CD (Lu, Chong-Dao); Xu, YJ (Xu, Yan-Jun); Lu, CD
2016
Source PublicationCHEMICAL COMMUNICATIONS
Volume52Issue:5Pages:912-915
AbstractA carbamoyl anion-initiated cascade reaction with acylsilanes and imines has been used to rapidly construct substituted alpha-hydroxy-beta-amino amides. The Brook rearrangement-mediated cascade allows the formation of two C-C bonds and one O-Si bond in a single pot. Using this approach, a range of alpha-aryl alpha-hydroxy-beta-amino amides has been synthesized in high yields with excellent diastereoselectivities
DOI10.1039/c5cc08118a
Indexed BySCI
WOS IDWOS:000367614000011
Citation statistics
Cited Times:7[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.xjipc.cas.cn/handle/365002/4345
Collection资源化学研究室
Corresponding AuthorLu, CD
AffiliationChinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Key Lab Plant Resources & Chem Arid Zones, Urumqi 830011, Peoples R China;Changji Univ, Dept Chem & Appl Chem, Changji 831100, Peoples R China
Recommended Citation
GB/T 7714
Lin, CY ,Ma, PJ ,Sun, Z ,et al. Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted alpha-hydroxy-beta-amino amides[J]. CHEMICAL COMMUNICATIONS,2016,52(5):912-915.
APA Lin, CY ,Ma, PJ ,Sun, Z ,Lu, CD ,Xu, YJ ,&Lu, CD.(2016).Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted alpha-hydroxy-beta-amino amides.CHEMICAL COMMUNICATIONS,52(5),912-915.
MLA Lin, CY ,et al."Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted alpha-hydroxy-beta-amino amides".CHEMICAL COMMUNICATIONS 52.5(2016):912-915.
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