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851942-89-7

851942-89-7 Structure

851942-89-7 Structure
IdentificationBack Directory
[Name]

(S)-4,4-DIBUTYL-2,6-BIS(3,4,5-TRIFLUOROPHENYL)-4,5-DIHYDRO-3H-DINAPHTHO[7,6,1,2-CDE]AZEPINIUM BROMIDE
[CAS]

851942-89-7
[Synonyms]

(S)-4,4-Dibutyl-2,6-bis(3,4,5-trifluorophenyl)-4,5-dihydro-3H-dinaphtho[7,6,1,2-cde]azepiniumbromide
(S)-4,4-DIBUTYL-2,6-BIS(3,4,5-TRIFLUOROPHENYL)-4,5-DIHYDRO-3H-DINAPHTHO[7,6,1,2-CDE]AZEPINIUM BROMIDE
(S)-4,4-Dibutyl-2,6-bis(3,4,5-trifluorophenyl)-4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]azepiniuM broMide
(11bS)-(+)-4,4-Dibutyl-4,5-dihydro-2,6-bis(3,4,5-trifluorophenyl)-3H-dinaphth[2,1-c:1',2'-e]azepinium bromide Nagase purity
[Molecular Formula]

C42H36F6N.Br
[MDL Number]

MFCD09264271
[MOL File]

851942-89-7.mol
[Molecular Weight]

748.645
Chemical PropertiesBack Directory
[Melting point ]

224-229 °C
[form ]

Powder
[color ]

brown
Questions And AnswerBack Directory
[Reaction]

  1. 2nd Generation Maruoka chiral phase transfer catalyst, for enantioselective alkylation of α-amino acid derivatives, that is easily recovered for recycle by extraction with fluorous solvent.
  2. Catalyst for asymmetric conjugate addition of α-substituted-α-cyanoacetates to α,β-unsaturated acetylenic esters.
  3. Phase transfer catalyzed enantioselective α-alkylation.
  4. Asymmetric amination of β-keto esters.
  5. Diastereo- and enantioselective conjugate addition of α-substituted nitroacetates to maleimides.
  6. Cyclization of β-alkynyl hydrazines.
Reactions of 851942-89-7
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