180999-24-0

Upstream product

• 79069-14-0 tert-butyl [(1R)-1-(hydroxymethyl)-2-methylpropyl]carbamate 
• 882-33-7 diphenyldisulfane 
• 4276-09-9 (R)-2-amino-3-methylbutanol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 126301-18-6 [(2S)-2-(tert-butoxycarbonylamino)-3-methylbutyl]methanesulfonate 
• 108-98-5 thiophenol 

Downstream Products

• 180999-37-5 [(R)-1-((S)-Benzenesulfinylmethyl)-2-methyl-propyl]-carbamic acid tert-butyl ester 
• 181140-14-7 [(R)-1-((R)-Benzenesulfinylmethyl)-2-methyl-propyl]-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Functional analysis of an aspartate-based epoxidation catalyst with amide-to-alkene peptidomimetic catalyst analogues

Subtle exchange: Replacement of an amide function with alkene or fluoroalkene groups provides a new class of epoxidation catalysts (see scheme). The structure-dependent catalytic behavior of these isosteric peptides provides mechanistic insights in their mode of action. (Chemical Equation Presented).

Chiral β-amino sulfoxides. Synthesis, configurational assignment and conformational analysis based on X-ray, CD, 1H NMR and theoretical calculations

Enantiomerically pure u and l β-amino sulfoxides have been easily obtained from the respective homochiral α-amino alcohols. The absolute configuration at the created stereogenic centre was assigned by CD spectra and by X-ray analysis. Conformational analysis of the title compounds was carried out using quantum chemical energy-geometry optimization. Thus established conformational behavior explained the strongly configuration dependent NMR spectral patterns observed for the u and l diastereomers.