61447-86-7

Upstream product

• 61447-83-4 1-isopropenyl-cyclopentane-1r,2t-diol 
• 562-13-0 2,2-dimethyl-1,3-cyclohexanedione 
• 74-88-4 methyl iodide 
• 27332-52-1 2-Isopropenyl-cyclopentanol-⁽²⁾-on-⁽¹⁾ 
• 3008-40-0 cyclopentane-1,2-dione 
• 1193-55-1 2-methylcyclohexane-1,3-dione 

Downstream Products

• 562-13-0 2,2-dimethyl-1,3-cyclohexanedione 
• 352424-95-4 3-tert-butyldimethylsilyloxy-2,2-dimethylcyclohexanone 
• 106540-31-2 (+)-(S)-3-(tert-butyldimethylsiloxy)-2,2-dimethylcyclohexanone 
• 131011-11-5 C₅₀H₇₃ClO₇Si₂ 
• 131011-09-1 (1aR,4aS,7S,7aS)-7-[(R)-3-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-propyl]-3-[3,3-dimethyl-2-oxo-4-triethylsilanyloxy-cyclohex-(E)-ylidenemethyl]-4a,7-dimethyl-1a,2,4a,5,6,7-hexahydro-1-oxa-cyclopropa[d]indene-4-carboxylic acid methyl ester 
• 131011-10-4 C₄₄H₅₉ClO₇Si 

Relevant academic research and scientific papers

SUBSTITUTED DIAMINOPYRIMIDYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

Provided herein are diaminopyrimidyl Compounds having the following structures: wherein X, L, R1, and R2 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidyl Compound, and methods for treating or preventing PKC-theta-mediated disorders, or a condition treatable or preventable by inhibition of a kinase, for example, PKC-theta.

An NMR tool for cyclodextrin selection in enantiomeric resolution by high-performance liquid chromatography

Complexation-induced chemical shifts and diffusion coefficients (HR-DOSY) of enantiomers with native and derivatized cyclodextrins were used for calculations of the apparent binding constants of three cyclohexanone inclusion complexes. Correlations between these data and high-performance liquid chromatography were established, revealing that this approach can be applied as an alternative method to predict enantiomeric discrimination. Copyright