This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

. 2001 Oct 17;123(41):10099-100.

doi: 10.1021/ja011306o.

Room-temperature alkyl-alkyl Suzuki cross-coupling of alkyl bromides that possess beta hydrogens

M R Netherton¹, C Dai, K Neuschütz, G C Fu

Affiliations

PMID: 11592890
DOI: 10.1021/ja011306o

Room-temperature alkyl-alkyl Suzuki cross-coupling of alkyl bromides that possess beta hydrogens

M R Netherton et al. J Am Chem Soc. 2001.

. 2001 Oct 17;123(41):10099-100.

doi: 10.1021/ja011306o.

Authors

M R Netherton¹, C Dai, K Neuschütz, G C Fu

Affiliation

¹ Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

PMID: 11592890
DOI: 10.1021/ja011306o

No abstract available

PubMed Disclaimer

Similar articles

Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions.
Kirchhoff JH, Netherton MR, Hills ID, Fu GC. Kirchhoff JH, et al. J Am Chem Soc. 2002 Nov 20;124(46):13662-3. doi: 10.1021/ja0283899. J Am Chem Soc. 2002. PMID: 12431081
Room-temperature Stille cross-couplings of alkenyltin reagents and functionalized alkyl bromides that possess beta hydrogens.
Menzel K, Fu GC. Menzel K, et al. J Am Chem Soc. 2003 Apr 2;125(13):3718-9. doi: 10.1021/ja0344563. J Am Chem Soc. 2003. PMID: 12656600
Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides.
Zhou JS, Fu GC. Zhou JS, et al. J Am Chem Soc. 2003 Dec 3;125(48):14726-7. doi: 10.1021/ja0389366. J Am Chem Soc. 2003. PMID: 14640646
Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides.
Zhou J, Fu GC. Zhou J, et al. J Am Chem Soc. 2004 Feb 11;126(5):1340-1. doi: 10.1021/ja039889k. J Am Chem Soc. 2004. PMID: 14759182
Recent applications of polymer supported organometallic catalysts in organic synthesis.
Kann N. Kann N. Molecules. 2010 Sep 7;15(9):6306-31. doi: 10.3390/molecules15096306. Molecules. 2010. PMID: 20877224 Free PMC article. Review.

See all similar articles

Cited by

A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies.
Bissember AC, Levina A, Fu GC. Bissember AC, et al. J Am Chem Soc. 2012 Aug 29;134(34):14232-7. doi: 10.1021/ja306323x. Epub 2012 Aug 20. J Am Chem Soc. 2012. PMID: 22905894 Free PMC article.
Palladium-catalyzed ligand-promoted site-selective cyanomethylation of unactivated C(sp³)-H bonds with acetonitrile.
Liu Y, Yang K, Ge H. Liu Y, et al. Chem Sci. 2016 Apr 21;7(4):2804-2808. doi: 10.1039/c5sc04066c. Epub 2016 Jan 6. Chem Sci. 2016. PMID: 28660057 Free PMC article.
Synthesis of Bridged Cyclopentane Derivatives by Catalytic Decarbonylative Cycloaddition of Cyclobutanones and Olefins.
Zhou X, Ko HM, Dong G. Zhou X, et al. Angew Chem Int Ed Engl. 2016 Oct 24;55(44):13867-13871. doi: 10.1002/anie.201608158. Epub 2016 Oct 6. Angew Chem Int Ed Engl. 2016. PMID: 27712025 Free PMC article.
Catalytic, enantioselective, intramolecular carbosulfenylation of olefins. Preparative and stereochemical aspects.
Denmark SE, Jaunet A. Denmark SE, et al. J Org Chem. 2014 Jan 3;79(1):140-71. doi: 10.1021/jo4023765. Epub 2013 Dec 11. J Org Chem. 2014. PMID: 24328051 Free PMC article.
Palladium-catalyzed borylation of primary alkyl bromides.
Joshi-Pangu A, Ma X, Diane M, Iqbal S, Kribs RJ, Huang R, Wang CY, Biscoe MR. Joshi-Pangu A, et al. J Org Chem. 2012 Aug 3;77(15):6629-33. doi: 10.1021/jo301156e. Epub 2012 Jul 23. J Org Chem. 2012. PMID: 22774861 Free PMC article.

See all "Cited by" articles

Publication types

Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions
Actions

Grants and funding

R01-GM62871/GM/NIGMS NIH HHS/United States

LinkOut - more resources

Other Literature Sources
- The Lens - Patent Citations Database