1112844-80-0Relevant academic research and scientific papers
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
Formal total synthesis of (+)-didemniserinolipid B
Prasad, Kavirayani R.,Gandi, Vasudeva Rao
experimental part, p. 2848 - 2852 (2011/03/19)
The formal total synthesis of (+)-didemniserinolipid B, a marine tunicate possessing a 6,8-dioxabicyclo[3.2.1]octane framework, was accomplished starting from l-(+)-tartaric acid. The key transformations in the synthesis include the elaboration of a γ-hyd
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.
