(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

Base Information

Chemical Name:(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole
CAS No.:1438392-85-8
Molecular Formula:C₂₂H₂₂N₂O
Molecular Weight:330.429
Hs Code.:

Synonyms:(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

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Chemical Property of (4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

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Technology Process of (4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

There total 5 articles about (4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole 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: 82.0%

: 16886-07-0
1,3-diallyl-1H-indole

: 40814-66-2
(Z)-2-chloro-1-phenylethan-1-one oxime

: 1438392-85-8
(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

Guidance literature:: With copper(I) trifluoromethanesulfonate * 1/2 toluene; (S)-2,2'-bis-1,1'-binaphthyl; silver carbonate; In dichloromethane; at 0 ℃; for 48h; Molecular sieve; Inert atmosphere;
DOI:10.1039/c6ob01149g

Reference yield: 82.0%

: 16886-07-0
1,3-diallyl-1H-indole

: 21572-32-7
2-chloro-1-phenyl-ethanone oxime

: (4aS,9aS)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

: 1438392-85-8
(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

Guidance literature:: With silver (II) carbonate; 2CF₃O₃S^(1-)*Cu⁽²⁺⁾*0.5C₇H₈; (S)-2,2'-bis-1,1'-binaphthyl; In dichloromethane; at -78 - 23 ℃; for 48h; Reagent/catalyst; enantioselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/chem.201203435

Reference yield:

: 16886-07-0
1,3-diallyl-1H-indole

: 14181-72-7,17082-13-2,17082-14-3
2-bromo-1-phenyl-ethanone oxime

: (4aS,9aS)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

: 1438392-85-8
(4aR,9aR)-4a,9-diallyl-3-phenyl-4,4a,9,9a-tetrahydro-[1,2]oxazino[6,5-b]indole

Guidance literature:: With silver (II) carbonate; 2CF₃O₃S^(1-)*Cu⁽²⁺⁾*0.5C₇H₈; (S)-(1,1'-binaphthalene)-2,2'-diylbis(diphenylphosphine); In dichloromethane; at -78 - 23 ℃; for 48h; Reagent/catalyst; Overall yield = 82 %; enantioselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/chem.201203435