268750-40-9

Upstream product

• 31469-16-6 1-ethoxy-1-((trimethylsilyl)oxy)-2-methylpropene 
• 268750-39-6 (3RS,5SR)-3,5-dibenzyloxy-4,4-dimethylheptane-1,7-dial 
• 268750-37-4 6-benzyloxy-5,5-dimethyl-1,8-nonadiene-4-one 
• 446264-32-0 5,5-dimethyl-1,8-nonadiene-4,6-diol 
• 100-39-0 benzyl bromide 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 1185-34-8 2,2-dimethylmalonaldehyde 
• 268750-38-5 (4RS,6SR)-4,6-dibenzyloxy-5,5-dimethyl-1,8-nonadiene 

Downstream Products

• 268750-41-0 (3RS,5RS,7SR,9SR)-5,7-dibenzyloxy-2,2,6,6,10,10-hexamethylundecane-1,3,9,11-tetraol 

Relevant academic research and scientific papers

Conformational analysis of oligo-1,3-dioxanylmethanes

Stereoselective synthesis of a series of 1,3-dioxan-4-ylmethanes 1-9 has been achieved by use of solely substrate-based asymmetric induction. The simple C2-symmetric bis(dioxanyl)methane 1 has a greater than 99% conformational preference at the two inter-ring bonds for the conformation 1a. The homologous structures 3-9 contain up to five dioxanylmethane units, maintaining a high conformational preference in each of the bis(dioxanyl)methane units. Thus, these flexible compounds reach a conformational preference in excess of 90% over up to eight rotatable interring bonds. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

Stereoselective synthesis of skipped polyols by substrate-directed asymmetric induction

(formula presented) A series of C2-or σ-symmetric oligo-1,3-dioxanylmethanes, 2-5, have been prepared using a bidirectional approach. In bidirectional syntheses of meso compounds, only substrate-based asymmetric induction could be applied. 1,3-