397251-81-9

Upstream product

• 100-39-0 benzyl bromide 
• 35192-73-5 (R)-non-1-en-4-ol 
• 66-25-1 hexanal 
• 31280-60-1 (S)-(-)-α-(Trimethylsilyl)benzenemethanol 
• 5908-41-8 benzoyltrimethylsilane 
• 397251-74-0 [(S)-((R)-1-Allyl-hexyloxy)-phenyl-methyl]-trimethyl-silane 
• 397251-71-7 (S)-α-(trimethylsilyloxy)benzyltrimethylsilane 
• 17921-71-0 (α,α-dibromotolyl)-α-trimethylsilane 
• 770-09-2 benzyltrimethylsilane 

Downstream Products

• 1403934-36-0 tert-butyl (R,E) 5-(benzyloxy)dec-2-enoate 
• 1403934-21-3 methyl (R,R,R)-3-[N-(3′-chloropropyl)-N-(α-methylbenzyl)amino]-5-(benzyloxy)decanoate 
• 1403934-23-5 methyl (R,R,R)-3-[N-(3'-azidopropyl)-N-(α-methylbenzyl)amino]-5-(benzyloxy)decanoate 
• 1403934-25-7 C₂₉H₄₄N₂O₃ 
• 1403934-27-9 (R,R,R)-4-[2′-(benzyloxy)heptyl]-N(5)-(α-methylbenzyl)-1,5-diazocan-2-one 
• 49620-05-5 (4′S,4''R,2'''R)-1-[2'-oxo-4′-phenyl-N(5')-methyl-1',5'-diazocan-N(1′)-yl]-4-[2''-oxo-4''-(2'''-hydroxyheptyl)-N(5'')-methyl-1'',5''-diazocan-N(1'')-yl]butane 

Relevant academic research and scientific papers

Absolute configuration assignment by asymmetric syntheses of the homalium alkaloids (?)-(R, R, R)-hoprominol and (?)-(4′ S,4″ R,2? R)-Hopromalinol

The conjugate addition of lithium (R)-N-(3-chloropropyl)-N-(α- methylbenzyl)amide to α,β-unsaturated esters was used as the key step in the syntheses of all possible diastereoisomers of the homalium alkaloids hoprominol and hopromalinol. Comparison of the

Optically pure α-(trimethylsilyl)benzyl alcohol: A practical chiral auxiliary for oxocarbenium ion reactions

(matrix presented) Enantiopure (S)-α-(trimethylsilyl)benzyl alcohol (98% ee) was prepared by Noyori's transfer hydrogenation of benzoyltrimethylsilane. The corresponding trimethylsilyl ether was subjected to Marko's silyl modified Sakurai conditions with