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

. 2007;46(26):4968-71.

doi: 10.1002/anie.200701215.

Reactivity of "frustrated Lewis pairs": three-component reactions of phosphines, a borane, and olefins

Jenny S J McCahill¹, Gregory C Welch, Douglas W Stephan

Affiliations

PMID: 17526043
DOI: 10.1002/anie.200701215

Reactivity of "frustrated Lewis pairs": three-component reactions of phosphines, a borane, and olefins

Jenny S J McCahill et al. Angew Chem Int Ed Engl. 2007.

. 2007;46(26):4968-71.

doi: 10.1002/anie.200701215.

Authors

Jenny S J McCahill¹, Gregory C Welch, Douglas W Stephan

Affiliation

¹ Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario, N9B 3P4, Canada.

PMID: 17526043
DOI: 10.1002/anie.200701215

No abstract available

PubMed Disclaimer

Similar articles

Frustrated Lewis pairs: metal-free hydrogen activation and more.
Stephan DW, Erker G. Stephan DW, et al. Angew Chem Int Ed Engl. 2010;49(1):46-76. doi: 10.1002/anie.200903708. Angew Chem Int Ed Engl. 2010. PMID: 20025001
1,4-Addition reactions of frustrated Lewis pairs to 1,3-dienes.
Ullrich M, Seto KS, Lough AJ, Stephan DW. Ullrich M, et al. Chem Commun (Camb). 2009 May 7;(17):2335-7. doi: 10.1039/b901212e. Epub 2009 Mar 6. Chem Commun (Camb). 2009. PMID: 19377677
Exploring the reactivity of carbon(0)/borane-based frustrated Lewis pairs.
Alcarazo M, Gomez C, Holle S, Goddard R. Alcarazo M, et al. Angew Chem Int Ed Engl. 2010 Aug 2;49(33):5788-91. doi: 10.1002/anie.201002119. Angew Chem Int Ed Engl. 2010. PMID: 20602390 No abstract available.
Tuning Lewis acidity using the reactivity of "frustrated Lewis pairs": facile formation of phosphine-boranes and cationic phosphonium-boranes.
Welch GC, Cabrera L, Chase PA, Hollink E, Masuda JD, Wei P, Stephan DW. Welch GC, et al. Dalton Trans. 2007 Aug 21;(31):3407-14. doi: 10.1039/b704417h. Epub 2007 May 17. Dalton Trans. 2007. PMID: 17664977
More than bystanders: the effect of olefins on transition-metal-catalyzed cross-coupling reactions.
Johnson JB, Rovis T. Johnson JB, et al. Angew Chem Int Ed Engl. 2008;47(5):840-71. doi: 10.1002/anie.200700278. Angew Chem Int Ed Engl. 2008. PMID: 18081111 Review.

See all similar articles

Cited by

Exploring Supramolecular Frustrated Lewis Pairs.
Hawkins PR, Hawes CS, Matthews PD. Hawkins PR, et al. Chempluschem. 2025 May;90(5):e202400725. doi: 10.1002/cplu.202400725. Epub 2025 Feb 11. Chempluschem. 2025. PMID: 39878090 Free PMC article. Review.
Synthesis of an oxygen-linked germinal frustrated Lewis pair and its application in small molecule activation.
Wang Y, Li ZH, Wang H. Wang Y, et al. RSC Adv. 2018 Jul 23;8(46):26271-26276. doi: 10.1039/c8ra05108a. eCollection 2018 Jul 19. RSC Adv. 2018. PMID: 35541977 Free PMC article.
Tri-insertion with dearomatization of terminal arylalkynes using a carborane based frustrated Lewis pair template.
Zhang J, Xie Z. Zhang J, et al. Chem Sci. 2020 Nov 28;12(5):1745-1749. doi: 10.1039/d0sc05755j. Chem Sci. 2020. PMID: 34163934 Free PMC article.
Advances in CO₂ activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions.
Khan MN, van Ingen Y, Boruah T, McLauchlan A, Wirth T, Melen RL. Khan MN, et al. Chem Sci. 2023 Nov 9;14(47):13661-13695. doi: 10.1039/d3sc03907b. eCollection 2023 Dec 6. Chem Sci. 2023. PMID: 38075657 Free PMC article. Review.
Σ- versus π-activation of alkynyl benzoates using B(C₆F₅)₃.
Bähr A, Wilkins LC, Ollegott K, Kariuki BM, Melen RL. Bähr A, et al. Molecules. 2015 Mar 12;20(3):4530-47. doi: 10.3390/molecules20034530. Molecules. 2015. PMID: 25774488 Free PMC article.

See all "Cited by" articles

LinkOut - more resources

Full Text Sources
- Wiley
Other Literature Sources
- The Lens - Patent Citations Database