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ChemicalBook >  Product Catalog >  Organic Chemistry >  Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4

Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4

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Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4 Basic information

Product Name:
Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4
Synonyms:
  • Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4
  • Rh2(S-PTAD)4
  • Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)
  • Rh2(S-PTAD)4
  • (2S)-2-(1-adamantyl)-2-(1,3-dioxoisoindol-2-yl)acetic acid,rhodium
  • Tetrakis[(S)-2-(1-adamantyl)-2-(1,3-dioxo-2-isoindolinyl)acetic Acid] Dirhodium(II)
CAS:
909389-99-7
MF:
C80H80N4O16Rh2
MW:
1559.34
Product Categories:
  • organometallic complex
  • Rh
Mol File:
909389-99-7.mol
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Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4 Chemical Properties

Melting point:
>300°C
alpha 
+39.1 (c 0.2, CHCl3)
form 
Powder
color 
green
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Tetrakis[(S)-(+)-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)Rh2(S-PTAD)4 Usage And Synthesis

Reaction

  1. Enantioselective reactions of carbenoids and olefins.
  2. Enantioselective C–H insertion reactions of carbenoids.
  3. Enantioselective oxygen transfer from diazosulfonylamidines. 

Uses

This chiral Rh(II) dimer was developed in the Davies lab to perform asymmetric carbene and nitrene reactions (C-H insertion, cyclopropanation, aziridination, C-H amination) with high regio- and stereocontrol.

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