Synthesis and evaluation of a chiral heterogeneous transfer hydrogenation catalyst.
Bayston DJ, et al.
Tetrahedron Asymmetry, 9(12), 2015-2018 (1998)
Nguyen-Hai Nam et al.
Bioorganic & medicinal chemistry, 12(22), 5753-5766 (2004-10-23)
A number of Src SH2 domain inhibitors enhance the kinase catalytic activity by switching the closed inactive to the open active conformation. ATP-phosphopeptide conjugates were designed and synthesized as Src tyrosine kinase inhibitors based on a tetrapeptide sequence pTyr-Glu-Glu-Ile (pYEEI)...
Mono-6-(O-2, 4, 6-triisopropylbenzenesulfonyl)-?-cyclodextrin, a novel intermediate for the synthesis of mono-functionalised ?-cyclodextrins.
Palin R, et al.
Tetrahedron Letters, 42(50), 8897-8899 (2001)