134824-01-4Relevant academic research and scientific papers
STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED 4a,8a-SUBSTITUTED 1,2,3,4,4a,6,8a,9,10,10a-DECAHYDROPHENANTHRENES, A NEW ENTRY TO THE QUASSINOID AND FUSIDANE FRAMEWORKS.
Vila, Alejandro J.,Cravero, Raquel M.,Gonzalez-Sierra, Manuel
, p. 4511 - 4526 (2007/10/02)
A series of highly functionalized angularly substituted bicyclic and tricyclic ketones were obtained regio- and stereoselectively by means of the Birch reductive alkylation on the properly functionalized benzylic ketones.
THE REDUCTIVE ALKYLATION OF AROMATIC KETONES REVISITED. A NEW STEREOSELECTIVE ROUTE TO HIGHLY FUNCTIONALIZED 4a,8a-SUBSTITUTED 1,2,3,4,4a,6,8a,9,10,10a-DECAHYDROPHENANTHRENES.
Vila, Alejandro J.,Cravero, Raquel M.,Gonzalez-Sierra, Manuel
, p. 1929 - 1932 (2007/10/02)
A series of highly functionalized angularly substituted bicyclic and tricyclic ketones were obtained regio- and stereoselectively by means of a Birch reductive alkylation.
