1089727-68-3Relevant academic research and scientific papers
Assessing synthetic strategies: Total syntheses of (±)- neodolabellane-type diterpenoids
Valente, Cory,Organ, Michael G.
supporting information; experimental part, p. 8239 - 8245 (2009/09/29)
Two strategies, namely a cross-metathesis/ring-closing metathesis and Pd-catalyzed Stille allylation/Nozaki-Hiyama-Kishi coupling, are examined for the preparation of neodolabellane-type diterpenoids 1 and 2. Whereas the first approach possessed synthetic
Oxazaborolidine-catalyzed enantioselective reduction of α-methylene ketones to allylic alcohols
Matsuo, Jun-Ichi,Kozai, Takaaki,Nishikawa, Osamu,Hattori, Yu,Ishibashi, Hiroyuki
, p. 6902 - 6904 (2008/12/22)
(Chemical Equation Presented) Oxazaborolidine-catalyzed enantioselective reduction of α-methylene ketones was efficiently carried out by using borane-diethylaniline as a stoichiometric reducing agent. The combination of this method and subsequent hydrogen
