21882-90-6

Upstream product

• 21882-89-3 (3-Benzyloxy-6-iodo-2,4-dimethoxy-phenyl)-acetonitrile 
• 20321-46-4 3-(benzyloxy)-2,4-dimethoxybenzaldehyde 
• 21882-87-1 4-Benzyloxy-3,5-dimethoxy-benzoyl azide 
• 866082-86-2 C₁₇H₁₇NO₃ 
• 14588-61-5 4-benzyloxy-3,5-dimethoxybenzoic acid chloride 
• 21882-88-2 2-Benzyloxy-4-chloromethyl-5-iodo-1,3-dimethoxy-benzene 
• 412014-23-4 2-benzyloxy-5-iodo-1,3-dimethoxy-benzene 
• 100-44-7 benzyl chloride 
• 32246-34-7 3-hydroxy-2,4-dimethoxy benzaldehyde 
• 121949-62-0 3-benzyloxy-2,4-dimethoxy-β-nitrostyrene 

Downstream Products

• 121949-63-1 5-benzyloxy-N-<2-(3'-benzyloxy-2',4'-dimethoxyphenyl)ethyl>-2-bromophenylacetamide 
• 21882-92-8 N-[2-(3-Benzyloxy-2,4-dimethoxy-phenyl)-ethyl]-2-(4-benzyloxy-phenyl)-acetamide 
• 121949-67-5 1-(2'-bromo-5'-hydroxybenzylidene)-2-carbethoxy-5,7-dimethoxy-6-hydroxy-1,2,3,4-tetrahydroisoquinoline 
• 121949-69-7 1-(2'-bromo-5'-hydroxybenzyl)-5,7-dimethoxy-6-hydroxy-3,4-dihydroisoquinoline hydrochloride 
• 121949-68-6 1-(5'-benzyloxy-2'-bromobenzylidene)-6-benzyloxy-2-carbethoxy-5,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 121985-85-1 6-benzyloxy-1-(5'-benzyloxy-2'-bromobenzyl)-5,7-dimethoxy-3,4-dihydroisoquinoline hydrochloride 
• 866082-87-3 C₂₂H₂₉NO₅ 
• 918414-78-5 C₂₀H₂₅NO₅ 

Relevant academic research and scientific papers

NITROGEN HETEROCYCLE BIARYLS FOR OSTEOPOROSIS AND OTHER DISEASES

Nitrogen heterocycle biaryls having a carboxylate terminus are useful for treating endometriosis, osteoporosis, restenosis following angioplasty, rheumatoid arthritis, cancer, macular degeneration and obesity. Compounds of formula: (I) are disclosed. A re

Nitrogen heterocycle biaryls for osteoporosis and other diseases

Nitrogen heterocycle biaryls having a carboxylate terminus are useful for treating endometriosis, osteoporosis, restenosis following angioplasty, rheumatoid arthritis, cancer, macular degeneration and obesity. Compounds of formula: are disclosed. A representative example is

Structure and synthesis of goudotianine, a new 7-methyldehydroaporphine from Guatteria goudotiana

Total synthesis of 2,9-dihydroxy-1,3-dimethoxy-7-methyl-6a,7-dehydroaporphine 1a and 3,9-dihydroxy-1,2-dimethoxy-7-methyl-6a,7-dehydroaporphine 1b are described. Direct comparison of both with natural goudotianine isolated from Guatteria goudotiana R.E. Fries showed the latter to be identical with 1b.