1352575-54-2

Upstream product

• 1420844-70-7 C₂₈H₂₁N₃O₅ 
• 1420844-71-8 C₂₈H₂₁N₃O₅ 
• 1420844-72-9 C₄₁H₄₀N₄O₈ 
• 1420844-73-0 C₃₆H₃₂N₄O₅ 
• 1420844-69-4 C₂₈H₂₁N₃O₄ 
• 151872-21-8 (R)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid methyl ester 
• 501-53-1 benzyl chloroformate 
• 1352575-51-9 C₃₆H₃₂N₄O₅ 
• 1352575-56-4 (2R,3aR,8aS)-8-benzyl 1-tert-butyl 3a-(1-((benzyloxy)carbonyl)-1H-indol-3-yl)-2-(methylcarbamoyl)-3,3a-dihydropyrrolo[2,3-b]indole-1,8(2H,8aH)-dicarboxylate 
• 1352575-50-8 (2R,3aR,8aS)-8-benzyl 1-tert-butyl 3a-(1H-indol-3-yl)-2-(methylcarbamoyl)-3,3a-dihydropyrrolo[2,3-b]indole-1,8(2H,8aH)-dicarboxylate 
• 1352575-49-5 (2R,3aR,8aS)-8-benzyl 1-tert-butyl 3a-(2-formyl-1H-indol-3-yl)-2-(methylcarbamoyl)-3,3a-dihydropyrrolo[2,3-b]indole-1,8(2H,8aH)-dicarboxylate 
• 1352575-48-4 (2R,3aS,8aS)-8-benzyl 1-tert-butyl 3a-bromo-2-(methylcarbamoyl)-3,3a-dihydropyrrolo[2,3-b]indole-1,8(2H,8aH)-dicarboxylate 
• 1352575-47-3 (2R,3aS,8aS)-8-benzyl 1-tert-butyl 2-methyl 3a-bromo-3,3a-dihydropyrrolo[2,3-b]indole-1,2,8(2H,8aH)-tricarboxylate 
• 1352575-55-3 (R)-benzyl 3-(2-((tert-butoxycarbonyl)amino)-3-methoxy-3-oxopropyl)-1H-indole-1-carboxylate 

Downstream Products

• 1352575-53-1 (5aS,10bR)-benzyl 10b-(1-((benzyloxy)carbonyl)-1H-indol-3-yl)-2-methyl-1,3,4-trioxo-3,4,5a,10b-tetrahydro-1H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-6(2H)-carboxylate 

Relevant academic research and scientific papers

Formal synthesis of (+)-gliocladin C

An asymmetric synthesis of chiral intermediate 15 for (+)-gliocladin C has been accomplished from N-phthaloyl l-tryptophan methyl ester.

Total synthesis of (+)-gliocladin C enabled by visible-light photoredox catalysis

Lighting the way: In a 10-step total synthesis of the title compound, visible-light photoredox catalysis enabled the construction of the key bond by facilitating the direct coupling of a pyrroloindoline-derived radical with a substituted indole (see schem