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애플리케이션
Dimethylzinc can be used as:
- A catalyst with nickel for the stereoselective C−2 alkenylation and dialkenylation of pyridine derivatives by alkynes to give monoalkenylation products.
- A reagent with aldehydes and 2-methoxyaniline for the enantioselective synthesis of alkyl and aralkyl secondary amines via one-pot three-component coupling reaction in the presence of zirconium tetraisopropoxide.
- A methylating reagent for the methylation of fluoroalkylated pyruvates in the presence of a copper/chiral diphosphine catalyst.
- An activator for radical trifluoromethylation of silyl enol ethers leading to α-trifluoromethyl ketones.
신호어
Danger
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 - STOT SE 3 - Water-react 1
표적 기관
Central nervous system
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 3
Flash Point (°F)
1.4 °F - closed cup
Flash Point (°C)
-17 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Radical trifluoromethylation of ketone silyl enol ethers by activation with dialkylzinc.
Organic Letters, 8(21), 4671-4673 (2006)
Organic letters, 8(21), 4671-4673 (2006-10-06)
[reaction: see text] The radical trifluoromethylation of ketone silyl enol ethers gave alpha-CF(3) ketones in good yields with wide scope of the ketonic substrates including acyclic ketones and cyclopentanone. The use of dialkylzinc to activate the silyl enol ethers is
Copper-catalyzed asymmetric methylation of fluoroalkylated pyruvates with dimethylzinc.
Beilstein Journal of Organic Chemistry, 14(1), 576-582 (2018)
Three-component catalytic asymmetric synthesis of aliphatic amines.
Journal of the American Chemical Society, 123(42), 10409-10410 (2001)
A strategy for C-H activation of pyridines: direct C-2 selective alkenylation of pyridines by Nickel/Lewis Acid catalysis.
Journal of the American Chemical Society, 130(8), 2448-2449 (2008)
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