1629094-38-7

Basic information

• Product Name: dimethyl (-)-(2S,2'S,3aS,3'aS,8aS,8'aS)-1,1'-bis{(S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenylpropanoyl}-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2-dicarboxylate
• Synonyms: dimethyl (-)-(2S,2'S,3aS,3'aS,8aS,8'aS)-1,1'-bis{(S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenylpropanoyl}-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2-dicarboxylate
• CAS NO: 1629094-38-7
• Molecular Weight: 957.136
• Mol File: 1629094-38-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dimethyl (-)-(2S,2'S,3aS,3'aS,8aS,8'aS)-1,1'-bis{(S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenylpropanoyl}-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl (-)-(2S,2'S,3aS,3'aS,8aS,8'aS)-1,1'-bis{(S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenylpropanoyl}-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2-dicarboxylate(1629094-38-7)
• EPA Substance Registry System: dimethyl (-)-(2S,2'S,3aS,3'aS,8aS,8'aS)-1,1'-bis{(S)-2-[tert-butoxycarbonyl(methyl)amino]-3-phenylpropanoyl}-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2-dicarboxylate(1629094-38-7)

Safety Data

• Hazardous Substances Data: 1629094-38-7(Hazardous Substances Data)

Upstream product

• 96238-68-5 tert-butyl (+)-(S)-3-[2-(tert-butoxycarbonylamino)-3-methoxy-3-oxopropyl]-1H-indole-1-carboxylate 
• 37553-65-4 Boc-N-Me-Phe-OH 
• 1629094-37-6 dimethyl (-)-(2S,2'S,3aS,3'aS,8aR,8'aR)-2,2',3,3',8,8a,8',8'a-octahydro-1H,1'H-3a,3'a-bipyrrolo[2,3-b]indole-2,2'-dicarboxylate 
• 1064604-21-2 methyl (2S,3aR,8aR)-[3a-bromo-(1,2,3,3a,8,8a)-hexahydropyrrolo[2,3-b]indole-1,8-di-tertbutoxycarbonyl]-2-carboxylate 
• 4299-70-1 L-tryptophan methyl ester 
• 73-22-3 L-Tryptophan 

Downstream Products

• 64947-43-9 (-)-ditryptophenaline 

Relevant articles and documents

Unified synthesis of (-)-folicanthine and (-)-ditryptophenaline enabled by a room temperature nickel-mediated reductive dimerization

A Ni·Phen-mediated reductive homocoupling of an optically active tertiary bromide has been efficiently achieved after the systematic screen of reaction conditions including ligands. This key step establishes sterically hindered vicinal quaternary stereocenters embedded in natural bispyrrolo[2,3-b]indoline alkaloids, thus enabling to realize the first asymmetric total synthesis of (-)-folicanthine via the detailed investigation of a challenging double decarboxylation. Notably, the concise synthesis of diketopiperazine alkaloid (-)-ditryptophenaline was also completed from the common dimeric intermediate. Georg Thieme Verlag Stuttgart New York.