444716-44-3Relevant academic research and scientific papers
Deleterious effect of 7-methyl group on glycosylation of 2-naphthols
Mitra, Prithiba,Mandal, Subhajit,Chakraborty, Soumen,Mal, Dipakranjan
, p. 5610 - 5619 (2015/08/03)
C-Glycosylations of several 2-naphthols with different glycosyl donors have been investigated in the pursuit of the total synthesis of mayamycin (1). While glycosylations of the parent 2-naphthol are readily achievable, those of 5-methoxy-7-methyl-2-napht
Regiospecific synthesis of a benanomicinone/pradimicinone analogue.
Hauser, Frank M,Liao, Hongbiao,Sun, Yuanqiang
, p. 2241 - 2243 (2007/10/03)
[reaction: see text] Condensation of a phenylsulfinyl naphthoate with an ortho-quinone monoketal has been used to accomplish a total synthesis of a benanomicinone/pradimicinone analogue.
