1.
Nat Prod Res
; 30(14): 1655-60, 2016 Jul.
Article
in English
| MEDLINE
| ID: mdl-26765952
ABSTRACT
A stereocontrolled, facile and high-yield approach for producing (+)-altroDNJ, has been developed starting from the inexpensive commercial cis 2-butene-1,4-diol. Sharpless epoxidation and a subsequent dihydroxylation were used for the introduction of all stereocentres; finally, the ring closure under basic conditions afforded the piperidine heterocycle.