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1372719-93-1

1372719-93-1 Structure

1372719-93-1 Structure
IdentificationBack Directory
[Name]

(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-phenanthrenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide
[CAS]

1372719-93-1
[Synonyms]

(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-phenanthrenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide
(11aR)-5-oxide-10,11,12,13-tetrahydro-5-hydroxy-3,7-di-9-phenanthrenyl-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9- phenanthrenyl-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2] dioxaphosphocin
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-phenanthrenyl-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin,99%e.e.
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-9-phenanthrenyl-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin, min. 98%
[Molecular Formula]

C45H32O4P
[MOL File]

1372719-93-1.mol
[Molecular Weight]

667.707
Chemical PropertiesBack Directory
[density ]

1.46
[form ]

Powder
[color ]

white to light-yellow
Questions and Answers (Q&A)Back Directory
[Reactions]

  1. Catalytic asymmetric homo-1,3-dipolar cycloadditions of azomethine ylides: diastereo and enantioselective synthesis of imidazolidines
  2. Enantioselective construction of the biologically significant dibenzo[1,4]diazepine scaffold via organocatalytic asymmetric three-component reactions
  3. Enantioselective construction of the biologically important cyclopenta[1,4]diazepine framework enabled by asymmetric catalysis by chiral spiro-phosphoric acid.
  4. Triply hydrogen-bond-directed enantioselective assembly of pyrrolobenzo-1,4-diazine skeletons with quaternary stereocenters.
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