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经验公式(希尔记法):
C32H56Cl2Rh2
化学文摘社编号:
分子量:
717.50
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
产品名称
双环辛烯氯化铑二聚体, 98%
SMILES string
Cl[Rh].Cl[Rh].C1CCCC=CCC1.C2CCCC=CCC2.C3CCCC=CCC3.C4CCCC=CCC4
InChI
1S/4C8H14.2ClH.2Rh/c4*1-2-4-6-8-7-5-3-1;;;;/h4*1-2H,3-8H2;2*1H;;/q;;;;;;2*+1/p-2/b4*2-1-;;;;
InChI key
GQPAPAIPOLEZHT-XFCUKONHSA-L
assay
98%
form
powder
reaction suitability
core: rhodium
reagent type: catalyst
mp
190 °C (dec.) (lit.)
Quality Level
Application
双环辛烯氯化铑(I)二聚体可用作以下反应的催化剂:
- 通过芳基硼酸与α,β-不饱和磺酰基化合物的不对称1,4-加成,合成富对映体的偕二芳基磺酸盐。
- N脱保护吲哚和吡咯的直接C-芳基化。
- 通过C-H键活化的在芳烃羧化反应。
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Rhodium (I)-catalyzed direct carboxylation of arenes with CO2 via chelation-assisted C- H bond activation
Mizuno H, et al.
Journal of the American Chemical Society, 133(5), 1251-1253 (2011)
Jay A Labinger et al.
Nature, 417(6888), 507-514 (2002-05-31)
The selective transformation of ubiquitous but inert C H bonds to other functional groups has far-reaching practical implications, ranging from more efficient strategies for fine chemical synthesis to the replacement of current petrochemical feedstocks by less expensive and more readily
Fumitoshi Kakiuchi et al.
Accounts of chemical research, 35(10), 826-834 (2002-10-16)
The cleavage and addition of ortho C-H bonds in various aromatic compounds such as ketones, esters, imines, imidates, nitrile, and aldehydes to olefins and acetlylenes can be achieved catalytically with the aid of ruthenium catalysts. The reaction is generally highly
Annulation of alkenyl-substituted heterocycles via rhodium-catalyzed intramolecular C-H activated coupling reactions.
K L Tan et al.
Journal of the American Chemical Society, 123(11), 2685-2686 (2001-07-18)
Ru-, Rh-, and Pd-catalyzed C-C bond formation involving C-H activation and addition on unsaturated substrates: reactions and mechanistic aspects.
Vincent Ritleng et al.
Chemical reviews, 102(5), 1731-1770 (2002-05-09)
商品
Discover the role of boronic acids in enantioenriched C(sp2)–C(sp2) product synthesis, specifically the rhodium-catalyzed Suzuki–Miyaura-type arylations of allylic halides and cyclobutenes.
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