808762-78-9Relevant academic research and scientific papers
Aromatic heterocycles as activating groups for asymmetric conjugate addition reactions. Enantioselective copper-catalyzed reduction of 2-alkenylheteroarenes
Rupnicki, Leszek,Saxena, Aakarsh,Hon, Wai Lam
supporting information; experimental part, p. 10386 - 10387 (2009/12/08)
(Chemical Equation Presented) The versatility of chiral copper hydride catalysis has been demonstrated through development of highly enantioselective 1,4-reductions of 2-alkenylheteroarenes, substrates that have been rarely considered for asymmetric conju
A concise synthesis of the functionalized [5-7-6] tricyclic skeleton of guanacastepene A
Du, Xiaohui,Chu, Hiufung V.,Kwon, Ohyun
, p. 8843 - 8846 (2007/10/03)
The six membered ring of guanacastepene A was constructed by a Diels-Alder reaction of 1,1,4-trisubstituted diene to set up the correct relative stereochemistry at the C8 quaternary center and the remote C5 stereocenter. In 10 efficient steps from the Die
