(6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

Base Information

Chemical Name:(6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole
CAS No.:1370549-67-9
Molecular Formula:C₂₆H₂₂N₂O₃
Molecular Weight:410.472
Hs Code.:

Synonyms:(6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

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Chemical Property of (6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

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Technology Process of (6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

There total 2 articles about (6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole 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:

Reference yield: 92.0%

: 92210-53-2
3-nitro-2H-1-benzopyran

: 81787-95-3
1-benzyl-2-vinyl-1H-indole

: 1370549-67-9
(6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

Guidance literature:: With C₄₂H₃₃N₃O₂; zinc trifluoromethanesulfonate; In toluene; at 20 ℃; for 20h; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/asia.201100820

Reference yield:

: 92210-53-2
3-nitro-2H-1-benzopyran

: 81787-95-3
1-benzyl-2-vinyl-1H-indole

: 1370549-67-9
(6aS,13cR)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

: 1370549-98-6
(6aR,13cS)-9-benzyl-6a-nitro-6,6a,7,8,9,13c-hexahydrochromeno[3,4-c]carbazole

Guidance literature:: With 2-[(4S,5S)-4,5-dihydro-4,5-diphenyl-2-oxazolyl]-N-[2-[(4S,5S)-4,5-dihydro-4,5-diphenyl-2-oxazolyl]phenyl]benzenamine; zinc trifluoromethanesulfonate; In toluene; at 20 ℃; for 26h; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/asia.201100820