603121-18-2

Upstream product

• 21382-82-1 (carbethoxyethylidene)triphenylphosphorane 
• 603121-09-1 (E)-(2S,3R,4R,5R,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4,6,8-tetramethyl-dec-8-enal 
• 213385-33-2 (R)-1-((4-methoxybenzyl)oxy)-2-methylpentan-3-one 
• 603121-10-4 (2S,4E)-2,4-dimethyl-4-hexenal 
• 603121-11-5 (E)-(S)-2,4-Dimethyl-hex-4-enoic acid methyl ester 
• 449174-20-3 methyl (R)-N-methyl-N-methoxy-3-(4-methoxybenzyloxy)-2-methylpropanoate 
• 603121-13-7 (E)-(2R,3S,4S,5R,6S)-1-(4-Methoxy-benzyloxy)-2,4,6,8-tetramethyl-dec-8-ene-3,5-diol 
• 603121-16-0 tert-Butyl-((E)-(1R,2S)-1-{(R)-1-[(2S,4S,5R)-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-ethyl}-2,4-dimethyl-hex-4-enyloxy)-dimethyl-silane 
• 603121-17-1 (E)-(2R,3S,4R,5R,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-2,4,6,8-tetramethyl-dec-8-en-1-ol 

Downstream Products

• 603121-21-7 tert-Butyl-[(5E,7E)-(1R,2R,3S,4R,10R)-1-((E)-(S)-1,3-dimethyl-pent-3-enyl)-3,11-bis-(4-methoxy-benzyloxy)-2,4,6,10-tetramethyl-undeca-5,7-dienyloxy]-dimethyl-silane 
• 603121-20-6 [(E)-(1R,2R,3S,4R)-7-Bromo-1-((E)-(S)-1,3-dimethyl-pent-3-enyl)-3-(4-methoxy-benzyloxy)-2,4,6-trimethyl-hept-5-enyloxy]-tert-butyl-dimethyl-silane 
• 603121-19-3 (2E,10E)-(4R,5S,6R,7R,8S)-7-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-2,4,6,8,10-pentamethyl-dodeca-2,10-dien-1-ol 

Relevant academic research and scientific papers

Total synthesis and structural elucidation of (-)-delactonmycin

The key steps in the total synthesis of delactonmycin (1) involved a Wittig olefination, a Negishi coupling, and an aldol reaction. The polyketide, which was isolated from Streptomyces sp., displays potent inhibitory activity of the nucleocytoplasmic tran