219654-10-1

Upstream product

• 917-54-4 methyllithium 
• 96481-69-5 (2S)-2-methyl-4-(benzyloxy)-1-butanal 
• 66261-30-1 (S)-4-(benzyloxy)-2-methylbutan-1-ol 

Downstream Products

• 219654-16-7 [(2R,3R)-3-((E)-(2R,7S)-9-Benzyloxy-2,6,7-trimethyl-4-methylene-non-5-enyl)-oxiranyl]-methanol 
• 219654-08-7 (E)-(S)-6-Benzyloxy-3,4-dimethyl-hex-2-enal 
• 1025839-70-6 (E)-(3S,8S)-4-Benzenesulfonyl-10-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-3,7,8-trimethyl-dec-6-en-5-ol 
• 219654-13-4 (E)-(3S,8S)-4-Benzenesulfonyl-10-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-3,7,8-trimethyl-dec-6-en-5-one 
• 219654-17-8 (E)-(3S,8S)-10-Benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-3,7,8-trimethyl-dec-6-en-5-one 
• 219654-14-5 ((E)-(3R,8S)-10-Benzyloxy-3,7,8-trimethyl-5-methylene-dec-6-enyloxy)-tert-butyl-diphenyl-silane 
• 219654-15-6 (2E,8E)-(5S,10S)-12-Benzyloxy-5,9,10-trimethyl-7-methylene-dodeca-2,8-dien-1-ol 
• 219654-07-6 (2R,3S)-3-((E)-(2R,7S)-9-Benzyloxy-2,6,7-trimethyl-4-methylene-non-5-enyl)-oxirane-2-carbaldehyde 

Relevant academic research and scientific papers

Asymmetric synthesis of 6′-hydroxyarenarol: The proposed biosynthetic precursor to popolohuanone E

(Chemical Equation Presented) The first synthesis of (+)-6′- hydroxyarenarol 3, the proposed biogenetic precursor to popolohuanone E (1), is described. An enantioselective route to key iodide intermediate 12 has been developed allowing the asymmetric synt

Synthetic studies toward potent cytotoxic agents amphidinolides: Synthesis of the C1-C18 moiety of amphidinolides G, H and L

Stereoselective synthesis of the (8S, 9S, 11R, 16S)-C1-C18 segment 1 of amphidinolides G, H and L, bearing the unique trisubstituted 's-cis-1,3- diene' moiety (C(28(29))=C13-C14=C15), has been achieved for the first time following a highly efficient convergent strategy.