Diversity-oriented synthesis of disubstituted alkenes using masked silanols
- PMID: 20491504
- DOI: 10.1021/ol100895d
Diversity-oriented synthesis of disubstituted alkenes using masked silanols
Abstract
The regio- and stereoselective synthesis and subsequent Hiyama cross coupling of pentafluorophenyldimethylvinylsilanes has been developed, thus providing a convenient and robust method for the diversity-oriented synthesis of (E)-, (Z)- and alpha-disubstituted alkenes from terminal alkynes. Pentafluorophenyldimethylvinylsilanes undergo cross-coupling reactions with excellent selectivity and in good yields, offering an attractive alternative to existing masked silanols.
Similar articles
-
Remarkable access to fluoroalkylated trisubstituted alkenes via highly stereoselective cobalt-catalyzed hydrosilylation reaction of fluoroalkylated alkynes.Org Biomol Chem. 2009 Mar 21;7(6):1167-70. doi: 10.1039/b819476a. Epub 2009 Jan 29. Org Biomol Chem. 2009. PMID: 19262936
-
Electrophilic trifluoromethylation by copper-catalyzed addition of CF3-transfer reagents to alkenes and alkynes.Org Lett. 2012 Jun 1;14(11):2882-5. doi: 10.1021/ol3011419. Epub 2012 May 21. Org Lett. 2012. PMID: 22612441
-
Stereoselective syntheses of trisubstituted olefins via platinum catalysis: alpha-silylenones with geometrical complementarity.J Am Chem Soc. 2010 Sep 1;132(34):11926-8. doi: 10.1021/ja1058197. J Am Chem Soc. 2010. PMID: 20690689
-
Catalytic synthesis of oligoene and enyne derivatives through carbometalation of internal alkynes.Chem Rec. 2008;8(5):326-36. doi: 10.1002/tcr.20158. Chem Rec. 2008. PMID: 18958852 Review.
-
Vinyl-, propargyl-, and allenylsilicon reagents in asymmetric synthesis: a relatively untapped resource of environmentally benign reagents.Chemistry. 2009;15(22):5402-16. doi: 10.1002/chem.200900337. Chemistry. 2009. PMID: 19421982 Review.
Cited by
-
(Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.Tetrahedron. 2011 Jun 17;67(24):4333-4343. doi: 10.1016/j.tet.2011.04.021. Tetrahedron. 2011. PMID: 22753994 Free PMC article. No abstract available.
-
An Expedient Regio- and Diastereoselective Synthesis of Hybrid Frameworks with Embedded Spiro[9,10]dihydroanthracene [9,3']-pyrrolidine and Spiro[oxindole-3,2'-pyrrolidine] Motifs via an Ionic Liquid-Mediated Multicomponent Reaction.Molecules. 2015 Sep 3;20(9):16142-53. doi: 10.3390/molecules200916142. Molecules. 2015. PMID: 26404224 Free PMC article.
-
Regioselective allene hydroarylation via one-pot allene hydrosilylation/Pd-catalyzed cross-coupling.Org Lett. 2014 Oct 17;16(20):5486-9. doi: 10.1021/ol502766q. Epub 2014 Oct 2. Org Lett. 2014. PMID: 25275880 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources