117 related articles for article (PubMed ID: 34734604)
1. Selective synthesis of enol ethers
Gong L; Zhang Q; Xie D; Zhang W; Xu SY; Zhang X; Niu D
Chem Commun (Camb); 2021 Nov; 57(92):12273-12276. PubMed ID: 34734604
[TBL] [Abstract][Full Text] [Related]
2. Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Oxo-vinylsulfones To Prepare C-Aryl Glycals and Acyclic Vinyl Ethers.
Gong L; Sun HB; Deng LF; Zhang X; Liu J; Yang S; Niu D
J Am Chem Soc; 2019 May; 141(19):7680-7686. PubMed ID: 31025860
[TBL] [Abstract][Full Text] [Related]
3. Dialkyl Ether Formation by Nickel-Catalyzed Cross-Coupling of Acetals and Aryl Iodides.
Arendt KM; Doyle AG
Angew Chem Int Ed Engl; 2015 Aug; 54(34):9876-80. PubMed ID: 26219537
[TBL] [Abstract][Full Text] [Related]
4. Stereospecific nickel-catalyzed cross-coupling reactions of benzylic ethers and esters.
Tollefson EJ; Hanna LE; Jarvo ER
Acc Chem Res; 2015 Aug; 48(8):2344-53. PubMed ID: 26197033
[TBL] [Abstract][Full Text] [Related]
5. Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents.
Binder JT; Cordier CJ; Fu GC
J Am Chem Soc; 2012 Oct; 134(41):17003-6. PubMed ID: 23039358
[TBL] [Abstract][Full Text] [Related]
6. Nickel catalyzed dealkoxylative C(sp2)-C(sp3) cross coupling reactions--stereospecific synthesis of allylsilanes from enol ethers.
Guo L; Leiendecker M; Hsiao CC; Baumann C; Rueping M
Chem Commun (Camb); 2015 Feb; 51(10):1937-40. PubMed ID: 25532100
[TBL] [Abstract][Full Text] [Related]
7. Exploration of new C-O electrophiles in cross-coupling reactions.
Yu DG; Li BJ; Shi ZJ
Acc Chem Res; 2010 Dec; 43(12):1486-95. PubMed ID: 20849101
[TBL] [Abstract][Full Text] [Related]
8. Direct Enol Ether Metalation-Negishi Coupling Strategy To Prepare α-Heteroaryl Enol Ethers.
Peng F; Liu K; Zhang H; Xu F; Liu Y; Shang G
Org Lett; 2023 Dec; 25(47):8516-8519. PubMed ID: 38037392
[TBL] [Abstract][Full Text] [Related]
9. Nickel-catalyzed Negishi alkylations of styrenyl aziridines.
Huang CY; Doyle AG
J Am Chem Soc; 2012 Jun; 134(23):9541-4. PubMed ID: 22414150
[TBL] [Abstract][Full Text] [Related]
10. Decarbonylative Cross-Couplings: Nickel Catalyzed Functional Group Interconversion Strategies for the Construction of Complex Organic Molecules.
Guo L; Rueping M
Acc Chem Res; 2018 May; 51(5):1185-1195. PubMed ID: 29652129
[TBL] [Abstract][Full Text] [Related]
11. Efficient Synthesis of Diaryl Ketones by Nickel-Catalyzed Negishi Cross-Coupling of Amides by Carbon-Nitrogen Bond Cleavage at Room Temperature Accelerated by a Solvent Effect.
Shi S; Szostak M
Chemistry; 2016 Jul; 22(30):10420-4. PubMed ID: 27304392
[TBL] [Abstract][Full Text] [Related]
12. 2,2-difluorovinyl benzoates for diverse synthesis of gem-difluoroenol ethers by Ni-catalyzed cross-coupling reactions.
Du B; Chan CM; Lee PY; Cheung LH; Xu X; Lin Z; Yu WY
Nat Commun; 2021 Jan; 12(1):412. PubMed ID: 33462244
[TBL] [Abstract][Full Text] [Related]
13. Access to β-Ketonitriles through Nickel-Catalyzed Carbonylative Coupling of α-Bromonitriles with Alkylzinc Reagents.
Donslund AS; Neumann KT; Corneliussen NP; Grove EK; Herbstritt D; Daasbjerg K; Skrydstrup T
Chemistry; 2019 Jul; 25(42):9856-9860. PubMed ID: 31162751
[TBL] [Abstract][Full Text] [Related]
14. Nickel-Catalyzed Reductive Conjugate Addition of Primary Alkyl Bromides to Enones To Form Silyl Enol Ethers.
Huihui KM; Shrestha R; Weix DJ
Org Lett; 2017 Jan; 19(2):340-343. PubMed ID: 28054785
[TBL] [Abstract][Full Text] [Related]
15. Expanding the chemical space of enol silyl ethers: catalytic dicarbofunctionalization enabled by iron catalysis.
Sar D; Yin S; Grygus J; Rentería-Gómez Á; Garcia M; Gutierrez O
Chem Sci; 2023 Nov; 14(45):13007-13013. PubMed ID: 38023494
[TBL] [Abstract][Full Text] [Related]
16. Nickel-Catalyzed Reductive 2-Pyridination of Aryl Iodides with Difluoromethyl 2-Pyridyl Sulfone.
Miao W; Ni C; Xiao P; Jia R; Zhang W; Hu J
Org Lett; 2021 Feb; 23(3):711-715. PubMed ID: 33417469
[TBL] [Abstract][Full Text] [Related]
17. Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond Activation.
Tobisu M; Chatani N
Top Curr Chem (Cham); 2016 Aug; 374(4):41. PubMed ID: 27573393
[TBL] [Abstract][Full Text] [Related]
18. Cross-Couplings Using Aryl Ethers via C-O Bond Activation Enabled by Nickel Catalysts.
Tobisu M; Chatani N
Acc Chem Res; 2015 Jun; 48(6):1717-26. PubMed ID: 26036674
[TBL] [Abstract][Full Text] [Related]
19. Selective iron-catalyzed cross-coupling reactions of grignard reagents with enol triflates, acid chlorides, and dichloroarenes.
Scheiper B; Bonnekessel M; Krause H; Fürstner A
J Org Chem; 2004 May; 69(11):3943-9. PubMed ID: 15153029
[TBL] [Abstract][Full Text] [Related]
20. Bench-Stable Electrophilic Fluorinating Reagents for Highly Selective Mono- and Difluorination of Silyl Enol Ethers.
Adachi A; Aikawa K; Ishibashi Y; Nozaki K; Okazoe T
Chemistry; 2021 Aug; 27(46):11919-11925. PubMed ID: 34009678
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]