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pro vyhledávání: '"Johnny H. Phan"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2895-2901 (2017)
A new method for imine synthesis by way of quinone-catalyzed oxidative deformylation of 1,2-amino alcohols is reported. A wide range of readily accessible amino alcohols and primary amines can be reacted to provide N-protected imine products. The met
Externí odkaz:
https://doaj.org/article/481607032a1e481abbf6a8cf2e91b109
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 2895-2901 (2017)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A new method for imine synthesis by way of quinone-catalyzed oxidative deformylation of 1,2-amino alcohols is reported. A wide range of readily accessible amino alcohols and primary amines can be reacted to provide N-protected imine products. The met
Publikováno v:
Chemical communications (Cambridge, England). 53(21)
A new method for amino acid homologation by way of formal C–C bond functionalization is reported. This method utilizes a 2-step/1-pot protocol to convert α-amino acids to their corresponding N-protected β-amino esters through quinone-catalyzed ox