477351-72-7

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 477351-61-4 (2S,3aR,5S,6S,7aS)-5,6-Dihydroxy-octahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 477351-56-7 (2S,4S,5S)-4,5-Diallyl-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 
• 477351-59-0 (1aR,2aR,4S,5aS,6aS)-Octahydro-1-oxa-5-aza-cyclopropa[f]indene-4,5-dicarboxylic acid 5-benzyl ester 4-methyl ester 
• 477351-57-8 (2S,3aS,7aS)-2,3,3a,4,7,7a-Hexahydro-indole-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester 

Downstream Products

• 477351-68-1 C₅₆H₈₆N₆O₁₃Si 
• 477351-80-7 (2S,3aR,5S,6S,7aS)-1-{(R)-2-[(R)-3-(tert-Butyl-diphenyl-silanyloxy)-2-methoxy-propionylamino]-4-methyl-pentanoyl}-5,6-bis-methoxymethoxy-octahydro-indole-2-carboxylic acid 
• 477351-67-0 (2S,3aR,5S,6S,7aS)-1-{(R)-2-[(R)-3-(tert-Butyl-diphenyl-silanyloxy)-2-methoxy-propionylamino]-4-methyl-pentanoyl}-5,6-bis-methoxymethoxy-octahydro-indole-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Total synthesis and structural confirmation of the marine natural product dysinosin A: A novel inhibitor of thrombin and Factor VIIa

The structure and absolute configuration of the marine antithrombotic product dysinosin A was confirmed by total synthesis. The strategy involved disconnections to three subunits, of which two were synthesized from the readily available l-glutamic acid, d