112460-48-7Relevant academic research and scientific papers
Synthetic studies related to CP-225,917
Clive, Derrick L.J.,Sgarbi, Paulo W.M.,He, Xiao,Sun, Shaoyi,Zhang, Junhu,Ou, Ligong
, p. 811 - 824 (2003)
Synthetic studies related to CP-225,917 are described, including the preparation of the fully oxygenated tetracyclic central core 3.
Robust synthesis of enantiopure cyclohexenyl analogues of 2/3-deoxyribose sugars as carbocyclic nucleoside precursors
Varada, Manojkumar,Kotikam, Venubabu,Kumar, Vaijayanti A.
experimental part, p. 5744 - 5749 (2011/08/21)
An expedient synthesis of 2-deoxy (10) and 3-deoxy (11) cyclohexenyl analogues of 2-deoxy and 3-deoxy-d-ribose sugar from commercially available starting materials is reported. Highly efficient enzymatic resolution of the key compound 10 is described usin
Microwave-assisted solvent-free Diels-Alder reaction - A fast and simple route to various 5,6-substituted norbornenes and polychlorinated norbornenes
Dejmek, Milan,Hrebabecky, Hubert,Sala, Michal,Drainsky, Martin,Nencka, Radim
experimental part, p. 4077 - 4083 (2012/01/05)
A series of 5,6-substituted norbornenes and 5,6-substituted polychlorinated norbornenes was prepared by using a microwave-assisted Diels-Alder reaction. This procedure proved very versatile, fast, and with an easy workup step, and therefore suitable even for large-scale synthesis. Georg Thieme Verlag Stuttgart · New York.
