RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 2004(6): 935-941
DOI: 10.1055/s-2004-822313
DOI: 10.1055/s-2004-822313
PAPER
© Georg Thieme Verlag Stuttgart · New York
General Synthesis and Catalytic Applications of Di(1-adamantyl)alkylphosphines and their Phosphonium Salts
Weitere Informationen
Received
4 February 2004
Publikationsdatum:
23. März 2004 (online)
Publikationsverlauf
Publikationsdatum:
23. März 2004 (online)
Abstract
An improved synthesis of di(1-adamantyl)alkylphosphines by alkylation of di(1-adamantyl)phosphine followed by deprotonation of the resulting phosphonium halide is described. Compared to previous protocols for the synthesis of this class of compounds, the procedure does not require chlorination of the secondary phosphine by phosgene, or formation of sensitive lithium di(1-adamantyl)phosphide. Selected examples of the prepared phosphonium salts and phosphines are shown to be excellent ligands for the palladium-catalyzed cross-coupling reaction of chloroarenes with arylboronic acids.
Key words
adamantylphosphines - aryl chlorides - palladium - phosphine ligands - Suzuki reaction
-
1a
Tsuji J. Palladium Reagents and Catalysts: Innovations in Organic Synthesis Wiley; Chichester: 1995. -
1b
Diederich F.Stang PJ. Metal Catalyzed Cross-Coupling Reactions Wiley-VCH; Weinheim: 1998. -
1c
Beller M.Bolm C. Transition Metals for Organic Synthesis Wiley-VCH; Weinheim: 1998. -
2a
Bedford RB.Cazin CSJ.Coles SJ.Gelbrich T.Hursthouse MB.Scordia VJM. Dalton Trans. 2003, 3350 -
2b
Kataoka N.Shelby Q.Stambuli JP.Hartwig JF. J. Org. Chem. 2002, 67: 5553 -
2c
Schnyder A.Indolese AF.Studer M.Blaser H.-U. Angew. Chem. Int. Ed. 2002, 41: 3668 ; Angew. Chem. 2002, 114, 3820 -
2d
Feuerstein M.Berthiol F.Doucet H.Santelli M. Synlett 2002, 1807 -
2e
Li GY. Angew. Chem. Int. Ed. 2001, 40: 1513 ; Angew. Chem. 2001, 113, 1561 -
2f
Gómez Andreu M.Zapf A.Beller M. Chem. Commun. 2000, 2475 -
2g
Zapf A.Beller M. Chem. Eur. J. 2000, 6: 1830 -
2h
Littke AF.Dai C.Fu GC. J. Am. Chem. Soc. 2000, 122: 4020 -
2i
Wolfe JP.Buchwald SL. Angew. Chem. Int. Ed. 1999, 38: 2413 ; Angew. Chem. 1999, 111, 2570 -
2j
Bei X.Turner HW.Weinberg WH.Guram AS.Petersen JL. J. Org. Chem. 1999, 64: 6797 -
2k
Beller M.Krauter JGE.Zapf A. Angew. Chem., Int. Ed. Engl. 1997, 36: 772 ; Angew. Chem. 1997, 109, 793 -
2l
Beller M.Fischer H.Herrmann WA.Öfele K.Broßmer C. Angew. Chem., Int. Ed. Engl. 1995, 34: 1848 ; Angew. Chem. 1995, 107, 1992 -
3a
Zapf A.Beller M. Chem. Eur. J. 2001, 7: 2908 -
3b
Stambuli JP.Stauffer SR.Shaughnessy KH.Hartwig JF. J. Am. Chem. Soc. 2001, 123: 2677 -
3c
Feuerstein M.Doucet H.Santelli M. J. Org. Chem. 2001, 66: 5923 -
3d
Morales-Morales D.Redón R.Yung C.Jensen CM. Chem. Commun. 2000, 1619 -
3e
Böhm VPW.Herrmann WA. Chem. Eur. J. 2000, 6: 1017 -
3f
Littke AF.Fu GC. J. Org. Chem. 1999, 64: 10 -
3g
Beller M.Zapf A. Synlett 1998, 792 -
3h
Reetz MT.Lohmer G.Schwickardi R. Angew. Chem. Int. Ed. 1998, 37: 481 ; Angew. Chem. 1998, 110, 492 -
3i
Albisson DA.Bedford RB.Lawrence SE.Scully PN. Chem. Commun. 1998, 2095 -
3j
Herrmann WA.Broßmer C.Reisinger C.-P.Öfele K.Beller M.Riermeier TH. Chem. Eur. J. 1997, 3: 1357 -
3k
Ohff M.Ohff A.van der Boom ME.Milstein D. J. Am. Chem. Soc. 1997, 119: 11687 -
4a
Bedford RB.Cazin CSJ.Coles SJ.Gelbrich T.Horton PN.Hursthouse MB.Light ME. Organometallics 2003, 22: 987 -
4b
Stambuli JP.Kuwano R.Hartwig JF. Angew. Chem. Int. Ed. 2002, 41: 4746 ; Angew. Chem. 2002, 114, 4940 -
4c
Wolfe JP.Buchwald SL. J. Org. Chem. 2000, 65: 1144 -
4d
Wolfe JP.Tomori H.Sadighi JP.Yin J.Buchwald SL. J. Org. Chem. 2000, 65: 1158 -
4e
Bei X.Uno T.Norris J.Turner HW.Weinberg WH.Guram AS. Organometallics 1999, 18: 1840 -
4f
Hamann BC.Hartwig JF. J. Am. Chem. Soc. 1998, 120: 3694 -
4g
Beller M.Riermeier TH.Reisinger C.-P.Herrmann WA. Tetrahedron Lett. 1997, 38: 2073 - 5
Littke AF.Fu GC. Angew. Chem. Int. Ed. 2002, 41: 4176 ; Angew. Chem. 2002, 114, 4350 - 6
Zapf A.Ehrentraut A.Beller M. Angew. Chem. Int. Ed. 2000, 39: 4153 ; Angew. Chem.; 2000, 112, 4315 - 7
Ehrentraut A.Zapf A.Beller M. Synlett 2000, 1589 - 8
Ehrentraut A.Zapf A.Beller M. J. Mol. Catal. 2002, 182-183: 515 - 9
Ehrentraut A.Zapf A.Beller M. Adv. Synth. Catal. 2002, 344: 209 -
10a
Beare NA.Hartwig JF. J. Org. Chem. 2002, 67: 541 -
10b
Stambuli JP.Kuwano R.Hartwig JF. Angew. Chem. Int. Ed. 2002, 41: 4746 ; Angew. Chem. 2002, 114, 4940 -
10c
Stambuli JP.Stauffer SR.Shaughnessy KH.Hartwig JF. J. Am. Chem. Soc. 2001, 123: 2677 -
11a
Köllhofer A.Pullmann T.Plenio H. Angew. Chem. Int. Ed. 2003, 42: 1056 ; Angew. Chem. 2003, 115, 1086 -
11b
Hillerich J.Plenio H. Chem. Commun. 2003, 3024 -
11c
Remmele H.Kollhofer A.Plenio H. Organometallics 2003, 22: 4098 -
11d
Kollhofer A.Plenio H. Chem. Eur. J. 2003, 9: 1416 -
12a
Benedí C.Bravo F.Uriz P.Fernández E.Claver C.Castillón S. Tetrahedron Lett. 2003, 44: 6073 -
12b
Schnyder A.Indolese AF.Studer M.Blaser H.-U. Angew. Chem. Int. Ed. 2002, 41: 3668 ; Angew. Chem. 2002, 114, 3820 -
12c
Schnyder A.Aemmer T.Indolese AF.Pittelkow U.Studer M. Adv. Synth. Catal. 2002, 344: 495 -
12d
Aranyos A.Old DW.Kiyomori A.Wolfe JP.Sadighi JP.Buchwald . J. Am. Chem. Soc. 1999, 121: 4369 -
13a
Goerlich JR.Schmutzler R. Phosphorus, Sulfur Silicon Relat. Elem. 1995, 102: 211 -
13b
Goerlich JR.Fischer A.Jones PG.Schmutzler R. Z. Naturforsch., B: Chem. Sci. 1994, 49: 801 -
13c
Goerlich JR.Schmutzler R. Phosphorus, Sulfur Silicon Relat. Elem. 1993, 81: 141 -
13d
Goerlich JR.Fischer A.Jones PG.Schmutzler R. Polyhedron 1993, 12: 2279 - 14 For other preparations of adamantylphosphines, see:
Ohashi A.Matsukawa S.Imamoto T. Heterocycles 2000, 52: 905 - 15
Netherton MR.Fu GC. Org. Lett. 2001, 3: 4295 -
16a
Leadbeater NE.Marco M. Angew. Chem. Int. Ed. 2003, 42: 1407 ; Angew. Chem. 2003, 115, 1445 -
16b
Leadbeater NE.Marco M. J. Org. Chem. 2003, 68: 5660