185628-40-4

Upstream product

• 1074-12-0 phenylglyoxal hydrate 
• 155324-36-0 (2'S,3'S,4S)-3-(3'-hydroxy-2'-methyl-4'-oxo-4'-phenylbutyryl)-4-isopropyl-2-oxazolidinone 
• 185628-39-1 Acetic acid (2S,3R)-2,4-diacetoxy-3-methyl-1-phenyl-butyl ester 

Downstream Products

• 126455-09-2 (2R,3R)-2-methyl-4-phenylbutane-1,3-diol 

Relevant academic research and scientific papers

Diastereo-face selectivity in the aldol reaction of boryl enolate derived from Oppolzer's sultam

In the Oppolzer aldol reaction, aldehyde reacts exclusively on the Si face (C(α)-Si attack) of the double bond of the boryl enolate 2 derived from (1S,2R)-N-propionylbornane-10,2-sultam (1), providing only 3a stereoselectively. Hexafluoroacetone (4) cause

Reversal of stereoselectivity in the Evans aldol reaction of α,α-difluoro and α,α,α-trifluoro carbonyl compounds

The Evans aldol reaction of hexafluoroacetone and trifluoroacetaldehyde causes complete reversal of diastereofacial selectivity. The boron enolate derived from N-acyloxazolidinone 2 reacts with trifluoroacetaldehyde to give anti and "non-Evans" syn aldols

Reversal of Stereoselectivity in the Aldol Reaction of Boron Enolate Derived from Oppolzer's Sultam with α,α-Difluoro and α,α,α-Trifluoro Carbonyl Compounds

Hexafluoroacetone causes the complete reversal of stereochemistry in the aldol reaction of boron enolate derived from Oppolzer's sultam in the absence of Lewis acids such as TiCl4.Trifluoroacetaldehyde and 2,2-difluoro-5-phenyl-1-pentanal cause partial re

Reversal of stereoselectivity in the Evans aldol reaction of α,α-difluoro and α,α,α-trifluoro carbonyl compounds

The Evans aldol reaction of hexafluoroacetone and trifluoroacetaldehyde causes reversal of stereoselectivity. The boron enolate derived from oxazolidinone 1 reacts with trifluoroacetaldehyde to give anti and "non-Evans" syn aldols with stereoselectivities