1112844-80-0Relevant articles and documents
Metal-mediated alkynediol cycloisomerization: First and second generation formal total syntheses of didemniserinolipid B
Das, Shyamsundar,Induvadana, Boddeti,Ramana
, p. 1881 - 1896 (2013/04/23)
A formal total synthesis of didemniserinolipid B was developed by employing a regioselective metal-mediated 6-endo-dig alkynol-cycloisomerization reaction. Two routes for the synthesis of key Burke's intermediate have been developed. Our initial approach
A formal synthesis of (+)-didemniserinolipid B employing a Pd-mediated 6-endo selective alkynediol cycloisomerization
Ramana,Induvadana, Boddeti
scheme or table, p. 271 - 273 (2009/04/11)
Herein, we describe a concise assembly of central 6,8-dioxabicyclo[3,2,1]octane core of didemniserinolipid by employing a Pd-mediated alkynediol cycloisomerization and a formal total synthesis of didemniserinolipid B.