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Tri-t-butylphosphine[bis(trifluoromethyl)sulfonylimido]gold(I), 98%

Catalog Number
ACM1121960937
Product Name
Tri-t-butylphosphine[bis(trifluoromethyl)sulfonylimido]gold(I), 98%
CAS
1121960-93-7
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Synonyms
MFCD21363047;Tri-t-butylphosphine[bis(trifluoromethyl)sulfonylimido]gold(I);1121960-93-7;
IUPAC Name
bis(trifluoromethylsulfonyl)azanide;gold(1+);tritert-butylphosphanium;
Molecular Weight
680.432g/mol
Molecular Formula
C14H28AuF6NO4PS2+;
Canonical SMILES
CC(C)(C)[PH+](C(C)(C)C)C(C)(C)C.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.[Au+];
InChI
InChI=1S/C12H27P.C2F6NO4S2.Au/c1-10(2,3)13(11(4,5)6)12(7,8)9;3-1(4,5)14(10,11)9-15(12,13)2(6,7)8;/h1-9H3;;/q;-1;+1/p+1;
InChI Key
DFDNDAVKAMVEPJ-UHFFFAOYSA-O;
Complexity
644
Covalently-Bonded Unit Count
3
Exact Mass
680.077g/mol
Formal Charge
1
H-Bond Acceptor
11
Heavy Atom Count
29
Monoisotopic Mass
680.077g/mol
Rotatable Bond Count
5
Topological Polar Surface Area
86A^2
Application
Catalyst used for the selective hydration of substituted alkynes at room temperature without acidic promoters.

Gold(I) catalyzes bromination of terminal alkynes.

Sequential O-H/C-H bond insertion of phenols initiated by the gold(I)-catalyzed cyclization of 1-bromo-1,5-enynes.

Ligand-controlled gold-catalyzed cycloisomerization of 1,n-enyne esters toward synthesis of dihydronaphthalene.
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