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(5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole

Base Information
  • Chemical Name:(5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole
  • CAS No.:1497405-21-6
  • Molecular Formula:C29H28N2
  • Molecular Weight:404.555
  • Hs Code.:
(5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole

Synonyms:(5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole

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Chemical Property of (5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole
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Technology Process of (5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole

There total 4 articles about (5aS,11aR)-5-benzyl-10-methyl-10,11-dihydro-5H-5a,11a-butanocyclopenta[1,2-b:3,4-b']diindole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin; In toluene; at 45 ℃; for 24h; enantioselective reaction;
DOI:10.1002/anie.201301618
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydroxide
2: hydrogen; palladium 10% on activated carbon
3: (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin / toluene / 24 h / 45 °C
With palladium 10% on activated carbon; (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin; hydrogen; sodium hydroxide; In toluene; 3: |Fischer Indole Synthesis;
DOI:10.1002/anie.201301618
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydroxide
2: hydrogen; palladium 10% on activated carbon
3: (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin / toluene / 24 h / 45 °C
With palladium 10% on activated carbon; (11aR)-10,11,12,13-tetrahydro-5-hydroxy-3,7-bis[2,4,6-triisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7’-fg][1,3,2]dioxaphosphocin; hydrogen; sodium hydroxide; In toluene; 3: |Fischer Indole Synthesis;
DOI:10.1002/anie.201301618
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