552298-30-3

Upstream product

• 552298-24-5 (2R,4S)-5-Benzyloxy-2,4-dimethyl-pentanoic acid ((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 
• 552298-26-7 ((2S,4R,6R)-7-Iodo-2,4,6-trimethyl-heptyloxymethyl)-benzene 
• 552298-25-6 ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene 
• 174627-70-4 (2R,4S,6S)-7-(benzyloxy)-2,4,6-trimethylheptan-1-ol 
• 169105-67-3 (2R,4S)-5-(benzyloxy)-2,4-dimethylpentan-1-ol 
• 90344-49-3 (2R)-3-iodo-2-methylpropyl benzyl ether 
• 63930-46-1 (S)-3-benzyloxy-2-methylpropan-1-ol 
• 3587-60-8 Benzyloxymethyl chloride 
• 64-17-5 ethanol 
• 552298-23-4 (2S,4R,6S,8S)-9-Benzyloxy-2,4,6,8-tetramethyl-nonanoic acid 
• 1027910-41-3 (2R,4R,6S)-7-Benzyloxy-2,4,6-trimethyl-heptanoic acid ((1S,2S)-2-hydroxy-1-methyl-2-phenyl-ethyl)-methyl-amide 

Downstream Products

• 552298-33-6 (4S,6R,8S,10S)-11-Benzyloxy-4,6,8,10-tetramethyl-3-triisopropylsilanyloxy-undecanenitrile 
• 552298-32-5 (4S,6R,8S,10S)-11-Benzyloxy-3-hydroxy-4,6,8,10-tetramethyl-undecanenitrile 
• 552298-31-4 (4S,6R,8S,10S)-11-Benzyloxy-4,6,8,10-tetramethyl-3-oxo-undecanenitrile 

Relevant academic research and scientific papers

Synthetic studies on borrelidin: enantioselective synthesis of the C1-C12 fragment.

[structure: see text] An efficient, enantioselective synthesis of the C1-C12 fragment 2 of borrelidin is presented. Construction of the "skipped" polymethylene chain of 2 was accomplished by iteration of Myers' alkylation, while formation of the C3 stereocenter was achieved by Roush's asymmetric allylboration methodology.