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Results: 1 to 20 of 118

1.

Copper-catalyzed coupling reaction of unactivated secondary alkyl iodides with alkyl Grignard reagents in the presence of 1,3-butadiene as an effective additive.

Shen R, Iwasaki T, Terao J, Kambe N.

Chem Commun (Camb). 2012 Sep 25;48(74):9313-5. doi: 10.1039/c2cc34847k. Epub 2012 Aug 13.

PMID:
22885657
[PubMed]
2.

Ni- or Cu-catalyzed cross-coupling reaction of alkyl fluorides with Grignard reagents.

Terao J, Ikumi A, Kuniyasu H, Kambe N.

J Am Chem Soc. 2003 May 14;125(19):5646-7.

PMID:
12733899
[PubMed]
3.

Co-catalyzed cross-coupling of alkyl halides with tertiary alkyl Grignard reagents using a 1,3-butadiene additive.

Iwasaki T, Takagawa H, Singh SP, Kuniyasu H, Kambe N.

J Am Chem Soc. 2013 Jul 3;135(26):9604-7. doi: 10.1021/ja404285b. Epub 2013 Jun 24.

PMID:
23782277
[PubMed - indexed for MEDLINE]
4.

Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes.

Terao J, Watanabe H, Ikumi A, Kuniyasu H, Kambe N.

J Am Chem Soc. 2002 Apr 24;124(16):4222-3.

PMID:
11960446
[PubMed]
5.

Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).

Terao J, Kambe N.

Acc Chem Res. 2008 Nov 18;41(11):1545-54. doi: 10.1021/ar800138a.

PMID:
18973349
[PubMed]
7.

Ni-catalyzed alkylative dimerization of vinyl grignard reagents using alkyl fluorides.

Terao J, Watabe H, Kambe N.

J Am Chem Soc. 2005 Mar 23;127(11):3656-7.

PMID:
15771474
[PubMed]
8.

Copper-catalyzed cross-coupling of nonactivated secondary alkyl halides and tosylates with secondary alkyl Grignard reagents.

Yang CT, Zhang ZQ, Liang J, Liu JH, Lu XY, Chen HH, Liu L.

J Am Chem Soc. 2012 Jul 11;134(27):11124-7. doi: 10.1021/ja304848n. Epub 2012 Jun 26.

PMID:
22734716
[PubMed]
9.

Mild and phosphine-free iron-catalyzed cross-coupling of nonactivated secondary alkyl halides with alkynyl Grignard reagents.

Cheung CW, Ren P, Hu X.

Org Lett. 2014 May 2;16(9):2566-9. doi: 10.1021/ol501087m. Epub 2014 Apr 22.

PMID:
24754234
[PubMed]
10.

Iron-copper cooperative catalysis in the reactions of alkyl Grignard reagents: exchange reaction with alkenes and carbometalation of alkynes.

Shirakawa E, Ikeda D, Masui S, Yoshida M, Hayashi T.

J Am Chem Soc. 2012 Jan 11;134(1):272-9. doi: 10.1021/ja206745w. Epub 2011 Dec 14.

PMID:
22128888
[PubMed]
11.
12.

Copper-catalyzed cross-coupling of functionalized alkyl halides and tosylates with secondary and tertiary alkyl Grignard reagents.

Ren P, Stern LA, Hu X.

Angew Chem Int Ed Engl. 2012 Sep 3;51(36):9110-3. doi: 10.1002/anie.201204275. Epub 2012 Jul 31.

PMID:
22855263
[PubMed]
13.

Copper-catalyzed alkyl-alkyl cross-coupling reactions using hydrocarbon additives: efficiency of catalyst and roles of additives.

Iwasaki T, Imanishi R, Shimizu R, Kuniyasu H, Terao J, Kambe N.

J Org Chem. 2014 Sep 19;79(18):8522-32. doi: 10.1021/jo501006u. Epub 2014 Jul 10.

PMID:
25010426
[PubMed - in process]
14.

Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.

Denmark SE, Cresswell AJ.

J Org Chem. 2013 Dec 20;78(24):12593-628. doi: 10.1021/jo402246h. Epub 2013 Nov 20.

PMID:
24256193
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Copper nanoparticle-catalyzed cross-coupling of alkyl halides with Grignard reagents.

Kim JH, Chung YK.

Chem Commun (Camb). 2013 Dec 7;49(94):11101-3. doi: 10.1039/c3cc46419a.

PMID:
24146018
[PubMed]
16.

Kumada-Corriu reactions of alkyl halides with alkynyl nucleophiles.

Yang LM, Huang LF, Luh TY.

Org Lett. 2004 Apr 29;6(9):1461-3.

PMID:
15101767
[PubMed]
17.

A Versatile Route to 2-Substituted Cyclic 1,3-Dienes via a Copper(I)-Catalyzed Cross-Coupling Reaction of Dienyl Triflates with Grignard Reagents.

Karlström AS, Rönn M, Thorarensen A, Bäckvall JE.

J Org Chem. 1998 Apr 17;63(8):2517-2522.

PMID:
11672113
[PubMed - as supplied by publisher]
18.

Silver-catalyzed benzylation and allylation reactions of tertiary and secondary alkyl halides with grignard reagents.

Someya H, Ohmiya H, Yorimitsu H, Oshima K.

Org Lett. 2008 Mar 6;10(5):969-71. doi: 10.1021/ol800038a. Epub 2008 Feb 2.

PMID:
18247499
[PubMed]
19.

Sequential one-pot addition of excess aryl-Grignard reagents and electrophiles to O-alkyl thioformates.

Murai T, Morikawa K, Maruyama T.

Chemistry. 2013 Sep 23;19(39):13112-9. doi: 10.1002/chem.201301573. Epub 2013 Aug 14.

PMID:
23946145
[PubMed]
20.

The Barbier-Grignard-type carbonyl alkylation using unactivated alkyl halides in water.

Keh CC, Wei C, Li CJ.

J Am Chem Soc. 2003 Apr 9;125(14):4062-3.

PMID:
12670223
[PubMed]
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