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US-Strem
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Product Information

Product Name
Chloro-1,5-cyclooctadiene iridium(I) dimer, 99%
Brand Name
US-Strem
Product Number
77-0400
CAS
12112-67-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
6436381
IUPAC Name
bis((1Z,5Z)-cycloocta-1,5-diene);bis(iridium);dichloride
InChI Key
SHZHQWGWORCBJK-MIXQCLKLSA-L
SMILES
C1/C=C\CC/C=C\C1.C1/C=C\CC/C=C\C1.Cl-.Cl-.Ir.Ir

Description

Technical Notes:
1.Precursor to catalysts for the asymmetric hydrogenation of tri- and tetrasubstituted olefins.
2.Precursor to catalyst for enantioselective reduction of imines.
3.Precursor to catalyst for allylic alkylation.
4.Precursor to catalyst for allylic amination and etherification.
5.Precursor to catalyst for the reaction of aroyl chlorides with internal alkynes to produce substituted naphthalenes and anthracenes.
6.Ir-catalyzed addition of acid chlorides to terminal alkynes.
7.Intramolecular hyd roamination of unactivated alkenes with secondary alkyI- and arylamines. 8.Enantioselective 2+ 2 cycloaddition.
9.Silyl-directed, Ir-catalyzed ortho-b orylation of arenes.
10.Ir-catalyzed cros s-coupling of styrene derivatives with allylic carbonates .
11.Transfer hydrogenative C-C coupling
References:
1.Angew. Chem. Int. Ed., 1998, 37, 2897.
2.J. Am. Chem. Soc., 1999, 121, 6421.
3.J. Am. Chem. Soc., 1998, 120, 8647. 4.J. Am. Chem. Soc, 2003, 125, 14272.
5.J. Am. Chem. Soc., 2002, 124, 12680.
6.J. Am. Chem. Soc, 2009, 131, 6668.
7.J. Am. Chem. Soc., 2010, 132, 413.
8.Org. L ett., 2010, 12, 304.
9.J. Am. Chem. Soc, 2008, 130, 7534.
10.J. Am. Chem. Soc., 2009, 131, 8346.
11.(a)J. Am. Chem. Soc., 2008, 130, 6340. (b) Angew. Chem. Int. Ed., 2009, 48, 6313.

References Data Source From Pubchem

Antifungal activity of rhodium, iridium, and ruthenium tripodal phosphine complexes

Publication Name: The new microbiologica
Publication Date: 2000-01