118378-11-3

Upstream product

• 118378-03-3 (1S,5S,6R,8S)-5-Benzyloxymethyl-8-(1-hydroxy-1-methyl-ethyl)-bicyclo[4.2.0]octan-2-one 
• 118378-04-4 (1R,5R,6S,8R)-5-Benzyloxymethyl-8-(1-methoxymethoxy-1-methyl-ethyl)-bicyclo[4.2.0]octan-2-one 
• 124665-36-7 [(1R,2aR,3R,8bR)-7-Amino-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,8b-hexahydro-cyclobuta[a]naphthalen-3-yl]-methanol 
• 118398-22-4 (1S,2aS,3S,8bS)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,8b-hexahydro-cyclobuta[a]naphthalen-7-ylamine 
• 124665-31-2 (1R,2aR,3R,8bR)-3-Benzyloxymethyl-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,8b-hexahydro-cyclobuta[a]naphthalen-7-ylamine 
• 118378-08-8 C₃₁H₅₁NO₄Si 
• 118378-07-7 N-[(1R,2aR,3R,8bR)-3-Benzyloxymethyl-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,8b-hexahydro-cyclobuta[a]naphthalen-7-yl]-benzamide 
• 124665-56-1 N-[(1S,2aS,3S,8bS)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,8b-hexahydro-cyclobuta[a]naphthalen-7-yl]-4-hydroxy-2,2-dimethyl-butyramide 
• 124665-34-5 (1R,2aR,3R,4aS,8bR)-3-Benzyloxymethyl-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,5,6,8b-octahydro-4aH-cyclobuta[a]naphthalen-7-one oxime 
• 118378-06-6 (1R,2aR,3R,4aS,8bR)-3-Benzyloxymethyl-1-(1-methoxymethoxy-1-methyl-ethyl)-8-methyl-1,2,2a,3,4,5,6,8b-octahydro-4aH-cyclobuta[a]naphthalen-7-one 
• 118378-09-9 C₃₁H₄₉NO₄Si 
• 124665-55-0 (1S,5S,6R,8S)-5-Benzyloxymethyl-3-[1-hydroxy-meth-(Z)-ylidene]-8-(1-methoxymethoxy-1-methyl-ethyl)-bicyclo[4.2.0]octan-2-one 
• 124665-50-5 (1R,2S,6S,7S)-2-Benzyloxymethyl-5,5-dimethoxy-bicyclo[4.2.0]octane-7-carboxylic acid methyl ester 
• 124665-33-4 (1R,2S,6S,7S)-2-Benzyloxymethyl-5-oxo-bicyclo[4.2.0]octane-7-carboxylic acid methyl ester 

Downstream Products

• 118378-12-4 C₂₉H₃₂N₂O₃Se 
• 118378-12-4 C₂₉H₃₂N₂O₃Se 

Relevant academic research and scientific papers

A Concise Route to the Penitrem Series of Tremorgenic Mycotoxins: Preparation of an Oxocane-Fused Indole

In this paper we record an efficient synthesis of tricyclic aniline 4, an advanced intermediated which embodies the B-C-D rings of penitrem D (1).In addition, a diminutive version of the natural product, hexacycle 10, was prepared.