362662-46-2

Upstream product

• 61654-68-0 2,5-bis-benzyloxy-1-bromo-3-methoxy-benzene 
• 420-37-1 trimethoxonium tetrafluoroborate 
• 163591-85-3 1,4-bis-(tert-butyl-dimethyl-silanyloxy)-but-2-yne 

Downstream Products

• 362662-52-0 1,5,8-tris-benzyloxy-2,3-bis(tert-butyldimethylsiloxymethyl)-4,6-dimethoxy-naphthalene 
• 362662-54-2 4,5,8-tris-benzyloxy-2-tert-butyldimethylsiloxymethyl-1,7-dimethoxy-3-methoxymethoxymethyl-naphthalene 
• 362662-61-1 [1,5,8-tris-benzyloxy-3-(tert-butyldimethylsiloxymethyl)-4,6-dimethoxy-naphthalen-2-yl]-methanol 
• 362662-58-6 4,5,8-tris-benzyloxy-2-tert-butyldimethylsiloxymethyl-1,7-dimethoxy-naphthalen-3-ol 
• 362662-53-1 1,5,8-tris-benzyloxy-3-(tert-butyldimethylsiloxymethyl)-4,6-dimethoxy-naphthalene-2-carbaldehyde 
• 362662-62-2 (4,5,8-tris-benzyloxy-1,7-dimethoxy-3-methoxymethoxymethyl-naphthalen-2-yl)-methanol 
• 362662-55-3 4,5,8-tris-benzyloxy-1,7-dimethoxy-3-methoxymethoxymethyl-naphthalene-2-carbaldehyde 
• 362662-56-4 4,5,8-tris-benzyloxy-1,7-dimethoxy-3-methoxymethoxymethyl-naphthalene-2-ol 

Relevant academic research and scientific papers

Synthesis of the naphthalene portion of the rubromycins.

[reaction: see text]. A synthesis of a reduced version of the naphthazarin found in the rubromycin class of natural products is reported. The naphthalene ring system is formed via a Doetz reaction with a symmetrical alkyne. Differentiation between the C1'