Chloro(tri-tert-butylphosphine)gold(I)

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Catalog Number
ACM69550283
Product Name
Chloro(tri-tert-butylphosphine)gold(I)
Structure
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CAS
69550-28-3
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Synonyms
Chlorogold;tritert-butylphosphane
IUPAC Name
chlorogold;tritert-butylphosphane;
Molecular Weight
434.73
Molecular Formula
C12H27AuClP
Canonical SMILES
CC(C)(C)P(C(C)(C)C)C(C)(C)C.Cl[Au]
InChI
InChI=1S/C12H27P.Au.ClH/c1-10(2,3)13(11(4,5)6)12(7,8)9;/h1-9H3;1H/q;+1;/p-1
InChI Key
JLXSZGSXDDQSJF-UHFFFAOYSA-M
Melting Point
>300 °C
Purity
99%
Complexity
130
Covalently-Bonded Unit Count
2
Exact Mass
434.120461
Heavy Atom Count
15
Monoisotopic Mass
434.120461
Rotatable Bond Count
3
Topological Polar Surface Area
0 Ų
Application
Chloro(tri-tert-butylphosphine)gold(I) serves as a versatile catalyst in a wide range of carbon-carbon bond-forming processes. It is particularly useful in cyclopropanation and plays a significant role in facilitating cycloisomerization reactions, such as those involving 2-(2-propynyl)pyridine N-oxides and 1,6-diynes. Additionally, it supports cycloisomerizations that conclude with sp3 C-H bond insertion. This catalyst also contributes to the synthesis of aromatic ketones through a transition metal-catalyzed tandem sequence, demonstrating its multifunctional capabilities in modern synthetic chemistry.
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