The first stereocontrolled synthesis of the unique calebassinine-1 skeleton has been developed utilising base-catalysed α-hydroxy ketone rearrangement as a key step.
Alpha-Hydroxy ketone rearrangement as a key step en route to the calebassinine skeleton / G. Palmisano, B. Danieli, G. Lesma, M. Mauro. - In: JOURNAL OF THE CHEMICAL SOCIETY, CHEMICAL COMMUNICATIONS. - ISSN 0022-4936. - :21(1986), pp. 1564-1565.
Alpha-Hydroxy ketone rearrangement as a key step en route to the calebassinine skeleton
B. DanieliSecondo
;G. LesmaPenultimo
;
1986
Abstract
The first stereocontrolled synthesis of the unique calebassinine-1 skeleton has been developed utilising base-catalysed α-hydroxy ketone rearrangement as a key step.
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