155486-11-6

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 21210-43-5 (S)-Methyl mandelate 
• 17199-29-0 (S)-Mandelic acid 

Downstream Products

• 94199-20-9 (S)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethanol 
• 141515-87-9 α,α'-di<(S)-2-hydroxy-2-phenylethyl>-o-xylenedioxide 
• 167355-62-6 α-<(R)-2-tetrahydropyranyloxy-2-phenylethyl>-α'-<(S)-2-tetrahydropyranyloxy-2-phenylethyl>-o-xylenedioxide 
• 167212-38-6 α,α'-bis<(S)-2-tetrahydropyranyloxy-2-phenylethyl>-o-xylenedioxide 
• 252044-69-2 O^α-(9-fluorenylmethyloxycarbonyl)-L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-73-8 O^α-(tetrahydropyran-2-yl)-L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-72-7 L-mandeloyl-L-mandeloyl-L-mandelic acid methyl ester 
• 252044-71-6 L-mandeloyl-D-mandeloyl-L-mandelic acid methyl ester 

Relevant academic research and scientific papers

CHIRAL SENSOR

An optically active compound having an unsaturated bond at an optically active binding site, wherein the unsaturated bond and a fluorescent substituent or a substituent capable of imparting fluorescence are united in a conjugated manner; and a chiral sens

Zirconium cation coordination in the borohydride-mediated synthesis of β-hydroxy-N-alkoxylamines

Hydride reductions of oxime ethers to hydroxylamine derivatives are facilitated by the participation of neighboring hydroxyl groups. Precomplexation with zirconium cation in ether-methylene chloride solutions is effective for selective C=N bond reduction. The course for stereochemical control is dictated by Lewis acid coordination complexes of E- and Z-oximino ethers which lead to the preferred diastereofacial delivery of external hydride.

A general methodology for automated solid-phase synthesis of depsides and depsipeptides. Preparation of a valinomycin analogue

A general methodology is described that allows the solid-phase synthesis of depsides and depsipeptides from chiral α-hydroxy- and α-amino acids. The results of studies with different protecting groups for the α-hydroxy acids and coupling systems for depsi

Enantioselective Protonation of Samarium Enolates by a C2-Symmetric Chiral Diol

High enantioselectivity (up to 97percentee) have been achieved in the protonation of samarium enolates which were generated by SmI2-mediated cross-coupling reaction between unsymmetrical dialkylketene and allyl iodide, using, using a C2-symmetr

Asymmetric Radical Reaction in the Coordination Sphere. IV. Ruthenium(II)-Catalyzed Asymmetric Addition of Sulfonyl Chloride to 1-Phenylpropene

The asymmetric addition of methane- and p-toluenesulfonyl chloride to 1-phenylpropene catalyzed by Ru2Cl43 affords optically active 1:1 adducts, (+)-(1R,2RS)-1-chloro-2-methylsulfonyl-1-phenylpropane (2) and (+)-(1R,2RS)-1-chloro-1-phenyl-2-tosy