1026419-29-3Relevant 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
Total synthesis of (±)-O-methyl PD 116740
Hauser, Frank M.,Dorsch, Warren A.,Mal, Dipakranjan
, p. 2237 - 2239 (2007/10/03)
(matrix presented) Condensation of the phthalide sulfide with an ortho-quinone monoketal was employed as a key step in the first total synthesis of a derivative of (±)-PD 116740.
