515844-79-8

Upstream product

• 100-39-0 benzyl bromide 
• 113427-43-3 1,4-di-O-benzyl-L-threitol 
• 868672-20-2 (2S,3S)-2,3-bis(phenylmethyloxy)-1,4-bis(methylsulfonyloxy)butane 
• 515844-78-7 (3S,4S)-3,4-Bis-benzyloxy-1-(toluene-4-sulfonyl)-pyrrolidine 

Downstream Products

• 1400575-85-0 C₅₄H₅₇N₃O₆ 
• 1400235-75-7 (3S,4S)-N-chloro-3,4-bis(benzyloxy)pyrrolidine 
• 869627-62-3 benzyl 4-{(3S,4S)-3,4-bis(benzyloxy)-pyrrolidin-1-yl}-benzoate 

Relevant academic research and scientific papers

Improving cytotoxic properties of ferrocenes by incorporation of saturated N-heterocycles

A family of ferrocene derivatives of the general formula [Fe(η5-C5H4CH2(p-C6H4)CH2(N-het))2] bearing saturated six- and five-membered N-heterocycles (N-het) was prepar

Design of branched and chiral solvatochromic probes: Toward quantifying polarity gradients in dendritic macromolecules

(Chemical Equation Presented) A pair of chiral, branched monomer building blocks, consisting of a solvatochromic probe and a spectroscopically inactive volume dummy, has been developed. The probe can selectively be excited, and its fluorescence characteristics provide information about local polarity. Incorporation of these monomers into high-generation polyester dendrimers should enable a detailed investigation of the polarity/density profile in dendritic architectures and ultimately allow for the realization of energy gradients from one chromophore building block only.

Phase-transfer-catalyzed asymmetric Michael reaction using newly-prepared chiral quaternary ammonium salts derived from L-tartrate

The catalytic asymmetric Michael reaction of a glycine Schiff base was demonstrated using new PTCs and moderate to good ee's were achieved (up to 77% ee).