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DOI: 10.1055/s-2006-956486
Chiral Thiophosphoramide and Thioamide Ligands in Catalytic Asymmetric Carbon-Carbon Bond-Formation Reactions
Publication History
Publication Date:
20 December 2006 (online)
Abstract
Metal complexes with organosulfur ligands exist widely in nature. The high polarizability of the electrons on the sulfur atoms is responsible for a variety of structures and the reactivity of metal complexes with sulfur-containing ligands. Organosulfur-containing chiral ligands have various applications in catalytic asymmetric reactions. Our group has been interested in the applications of a series of thiophosphoramide and thioamide ligands in asymmetric carbon-carbon bond-formation reactions. In this account, we describe the synthesis of chiral thiophosphoramide and thioamide ligands and their applications in catalytic asymmetric carbon-carbon bond formation.
1 Introduction
2 Synthesis of Chiral Organosulfur-Containing Ligands
3 Applications in Carbon-Carbon Bond-Formation Reactions
3.1 Conjugate Addition of Organozinc Reagents to Enones
3.2 Addition of Diethylzinc to Imines
3.3 Additon of Diethylzinc to Aldehydes
3.4 Addition of Allylic Stannane to Aldehydes
3.5 Other Applications
4 Conclusion
Key words
organosulfur-containing ligands - thiophosphoramide - thioamide - asymmetric carbon-carbon bond formation
- 1
Broderick JB. In Comprehensive Coordination Chemistry II Vol. 8:McCleverty JA.Meyer TJ. Elsevier-Pergamon; Amsterdam: 2004. p.739-757 - 2
King RB. In Iron Sulfur Proteins in Encyclopedia of Inorganic ChemistryJohnson MK. Wiley; Chichester: 1994. p.1896-1915 - 3
Beinert H.Holm RH.Munck E. Science 1997, 277: 653 - 4
Beinert H. J. Biol. Inorg. Chem. 2000, 5: 2 - 5
Comprehensive Coordination Chemistry
Vol. 2:
Wilkinson SG.Gillard RD.McCleverty JA. Elsevier-Pergamon; Amsterdam: 1987. p.515-659 -
6a
Pearson RG. J. Am. Chem. Soc. 1963, 85: 3533 -
6b
Pearson RG.Songstad J. J. Am. Chem. Soc. 1967, 89: 1827 -
6c
Pearson RG. In Hard and Soft Acids and Bases Dowden, Hutchinson and Ross; Stroudsberg: 1973. -
7a
Roos BO. Acc. Chem. Res. 1999, 32: 137 -
7b
Rodriguez JA.Hrbek J. Acc. Chem. Res. 1999, 32: 719 -
7c
Avalos M.Babiano R.Cintas P.Jimenez JL.Palacios JC. Acc. Chem. Res. 2005, 38: 460 -
8a
Grapperhaus CA.Darensbourg MY. Acc. Chem. Res. 1998, 31: 451 -
8b
Venkateswara Rao P.Holm RH. Chem. Rev. 2004, 104: 527 - 9
Vahrenkamp H. Angew. Chem., Int. Ed. Engl. 1975, 14: 322 -
10a
Kuehn CC.Taube H. J. Am. Chem. Soc. 1976, 98: 689 -
10b
Herberhold M.Suss G. Angew. Chem., Int. Ed. Engl. 1976, 15: 366 -
11a
Soai K.Niwa S. Chem. Rev. 1992, 92: 833 -
11b
Hof RP.Poelert MA.Peper NCMW.Kellogg RM. Tetrahedron: Asymmetry 1994, 5: 31 -
11c
Allen JV.Coote SJ.Dawson GJ.Frost CG.Martin CJ.Williams JMJ. J. Chem. Soc., Perkin Trans. 1 1994, 2065 -
11d
Orejon A.Masdeu-Bulto AM.Echarri R.Dieguez M.Fornies-Camer J.Claver C.Cardin CJ. J. Organomet. Chem. 1998, 559: 23 -
11e
Hiroi K.Suzuki Y. Tetrahedron Lett. 1998, 39: 6499 -
11f
Evans DA.Campos KR.Tedrow JS.Michael FE.Gagne MR. J. Org. Chem. 1999, 64: 2994 -
11g
Perales JB.van Vranken DL. J. Org. Chem. 2001, 66: 7270 -
12a
Knorr M.Strohmann C. Organometallics 1999, 18: 248 -
12b
Gbor PK.Ahmed IB.Jia CQ. Ind. Eng. Chem. Res. 2002, 41: 1861 -
13a
Berkessel A.Gröger H. In Metal-Free Organic Catalysts in Asymmetric Synthesis Wiley-VCH; Weinheim: 2004. - 13b Special issue: Asymmetric Organocatalysis, Acc. Chem. Res. 2004, 37: 487-631
- 13c Special feature: Asymmetric Catalysis, Proc. Natl. Acad. Sci. U.S.A. 2004, 101: 5347-5487
-
13d For selected reviews, see:
Dalko PI.Moisan L. Angew. Chem. Int. Ed. 2001, 40: 3726 -
13e
Benaglia M.Puglisi A.Cozzi F. Chem. Rev. 2003, 103: 3401 -
13f
Dalko PI.Moisan L. Angew. Chem. Int. Ed. 2004, 43: 5138 -
13g
Seayad J.List B. Org. Biomol. Chem. 2005, 3: 719 -
13h
Taylor MS.Jacobsen EN. Angew. Chem. Int. Ed. 2006, 45: 1520 - 14 For example, see:
Victoriano LI.Garland MT.Vega A. Inorg. Chem. 1997, 36: 688 - For example, see:
-
15a
Schrauzer GN. Acc. Chem. Res. 1969, 2: 72 -
15b
Bucheler J.Zeug N.Kisch H. Angew. Chem., Int. Ed. Engl. 1982, 21: 783 -
15c
Battaglia R.Henning R.Dinh-Ngoc B.Schlamann W.Kisch H. J. Mol. Catal. 1983, 21: 239 - 16
Li GY.Marshall WJ. Organometallics 2002, 21: 590 - For selected examples, see:
-
17a
Gilbertson SR.Chen G.McLoughlin M. J. Am. Chem. Soc. 1994, 116: 4481 -
17b
Gilbertson SR.Wang X. J. Org. Chem. 1996, 61: 434 -
17c
Gilbertson SR.Pawlick RV. Angew. Chem., Int. Ed. Engl. 1996, 35: 902 -
18a
Dawson GJ.Frost CG.Martin CJ.Williams JMJ.Coote SJ. Tetrahedron Lett. 1993, 34: 7793 -
18b
Allen JV.Bower JF.Williams JMJ. Tetrahedron: Asymmetry 1994, 5: 1895 -
18c
Sprinz J.Kiefer M.Helmchen G.Reggelin M.Huttner G.Walter O.Zsolnai L. Tetrahedron Lett. 1994, 35: 1523 -
18d
Morimoto T.Tachibana K.Achiwa K. Synlett 1997, 783 -
18e
Anderson JC.James DS.Mathias JP. Tetrahedron: Asymmetry 1998, 9: 753 -
18f
Boog-Wick K.Pregosin PS.Trabesinger G. Organometallics 1998, 17: 3254 -
19a
Kleijn H.Rijnberg E.Jastrzebski JTBH.van Koten G. Org. Lett. 1999, 1: 853 -
19b
Bergbreiter DE.Osburn PL.Frels JD. J. Am. Chem. Soc. 2001, 123: 11105 - 20
Soai K.Hirose Y.Ohno Y. Tetrahedron: Asymmetry 1993, 4: 1473 - 21
Soai K.Hatanaka T.Miyazawa T. J. Chem. Soc., Chem. Commun. 1992, 1097 -
22a
Soai K.Ohno Y.Inoue Y.Tsuruoka T.Hirose T. Recl. Trav. Chim. Pays-Bas 1995, 114: 145 -
22b
Hulst R.Heres H.Fitzpatrick K.Peper NCMW.Kellogg RM. Tetrahedron: Asymmetry 1996, 7: 2755 -
22c
Shibata T.Tabira H.Soai K. J. Chem. Soc., Perkin Trans. 1 1998, 177 - 23
Miyano S.Nawa M.Mori A.Hashimoto H. Bull. Chem. Soc. Jpn. 1984, 57: 2171 - 24
Pini D.Iuliano A.Rosini C.Salvadori P. Synthesis 1990, 1023 - 25
Mitchell JM.Finney NS. Tetrahedron Lett. 2000, 41: 8431 - 26
You J.-S.Shao M.-Y.Gau H.-M. Tetrahedron: Asymmetry 2001, 12: 2971 - 27
Klingsberg E.Papa D. J. Am. Chem. Soc. 1951, 73: 4988 -
28a
Perlmutter P. Conjugate Addition Reaction in Organic Synthesis, In Tetrahedron Organic Chemistry Series Vol. 9: Pergamon Press; Oxford: 1992. -
28b
Krause N.Hoffmann-Roder A. Synthesis 2001, 171 -
29a
Houri AF.Xu Z.Cogan DA.Hoveyda AH. J. Am. Chem. Soc. 1995, 117: 2943 -
29b
Lebel H.Jacobsen EN. J. Org. Chem. 1998, 63: 9624 -
29c
Han X.Corey EJ. Org. Lett. 1999, 1: 1871 -
29d
Fox ME.Li C.Marino JP.Overman LE. J. Am. Chem. Soc. 1999, 121: 5467 -
29e
Deng H.Jung J.-K.Liu T.Kuntz KW.Snapper ML.Hoveyda AH. J. Am. Chem. Soc. 2003, 125: 9032 -
29f
Cesati RR.de Armas J.Hoveyda AH. J. Am. Chem. Soc. 2004, 126: 96 -
30a
Shi M.Wang C.-J.Zhang W. Chem. Eur. J. 2004, 10: 5507 -
30b
Shi M.Zhang W. Adv. Synth. Catal. 2005, 347: 535 -
30c
Shi M.Zhang W. Tetrahedron: Asymmetry 2004, 15: 167 -
30d
Shi M.Duan W.-L.Gong G.-B. Chirality 2004, 16: 642 -
31a
Rudolph J.Rasmussen T.Bolm C.Norrby PO. Angew. Chem. Int. Ed. 2003, 42: 3002 -
31b
Kitamura M.Okada S.Suga S.Noyori R. J. Am. Chem. Soc. 1989, 111: 4028 -
32a
Schinnerl M.Seitz M.Kaiser A.Reiser O. Org. Lett. 2001, 3: 4259 -
32b
Bolm C.Hildebrand JP.Muniz K.Hermanns N. Angew. Chem. Int. Ed. 2001, 40: 3284 - 33
Alexakis A.Benhaim C. Eur. J. Org. Chem. 2002, 3221 - For selected X-ray structures for copper complexes coordinated by sulfur and nitrogen ligands, see:
-
34a
Knotter DM.Grove DM.Smeets WJJ.Spek AL.van Koten G. J. Am. Chem. Soc. 1992, 114: 3400 -
34b
Brubaker GR.Brown JN.Yoo MK.Kinsey RA.Kutchan TM.Mottel EA. Inorg. Chem. 1979, 18: 299 - 35
Lewis Acids in Organic Synthesis
Yamamoto H. Wiley-VCH; Weinheim: 2000. - For sulfur-based stable and recoverable ligands, see:
-
36a
Cunningham A.Woodward S. Synlett 2002, 43 -
36b
Fraser PK.Woodward S. Tetrahedron Lett. 2001, 42: 2747 -
36c
Borner C.Dennis MR.Woodward S. Eur. J. Org. Chem. 2001, 2435 -
36d
Fraser PK.Woodward S. Chem. Eur. J. 2003, 9: 776 -
37a
Wirth T. Tetrahedron 1999, 55: 1 -
37b
Nishibayashi Y.Segawa K.Singh JD.Fukuzawa S.-I.Ohe K.Uemura S. Organometallics 1996, 15: 370 -
37c
Nishibayashi Y.Singh JD.Arikawa Y.Uemura S.Hidai M. J. Organomet. Chem. 1997, 531: 13 -
37d
Fukuzawa S.-I.Tsudzuki K. Tetrahedron: Asymmetry 1995, 6: 1039 -
37e
Santi C.Wirth T. Tetrahedron: Asymmetry 1999, 10: 1019 -
37f
Nishibayashi Y.Singh JD.Segawa K.Fukuzawa S.-I.Uemura S. J. Chem. Soc., Chem. Commun. 1994, 1375 -
37g
Wirth T. Tetrahedron Lett. 1995, 36: 7849 -
37h
You S.-L.Hou X.-L.Dai L.-X. Tetrahedron: Asymmetry 2000, 11: 1495 -
38a
Kitamura M.Miki T.Nakano K.Noyori R. Bull. Chem. Soc. Jpn. 2000, 73: 999 -
38b
Nakano K.Bessho Y.Kitamura M. Chem. Lett. 2003, 32: 224 -
39a
Wynberg H.Feringa B. Tetrahedron 1976, 32: 2831 -
39b
Puchot C.Samuel O.Dunach E.Zhao S.Agami C.Kagan HB. J. Am. Chem. Soc. 1986, 108: 2353 -
39c
Oguni N.Matsuda Y.Kaneko T. J. Am. Chem. Soc. 1988, 110: 7877 -
39d
Guillaneux D.Zhao S.-H.Samuel O.Rainford D.Kagan HB. J. Am. Chem. Soc. 1994, 116: 9430 -
39e
Reggelin M. Nachr. Chem., Tech. Lab. 1997, 45: 392 - 40
Girard C.Kagan HB. Angew. Chem. Int. Ed. 1998, 37: 2922 - 41
Federsel H.-J.Collins AN.Sheldrake GN.Crosby J. In Chirality in Industry II John Wiley & Sons; Chichester: 1997. p.225-244 - For excellent reviews, see:
-
42a
Enders D.Reinhold U. Tetrahedron: Asymmetry 1997, 8: 1895 -
42b
Bloch R. Chem. Rev. 1998, 98: 1407 -
42c
Kobayashi S.Ishitani H. Chem. Rev. 1999, 99: 1069 -
43a
Denmark SE.Nakajima N.Nicaise OJ.-C. J. Am. Chem. Soc. 1994, 116: 8797 -
43b
Denmark SE.Stiff CM. J. Org. Chem. 2000, 65: 5875 -
43c
Tomioka K.Inoue I.Shindo M.Koga K. Tetrahedron Lett. 1991, 32: 3095 -
44a
Andersson PG.Guijarro D.Tanner D. J. Org. Chem. 1997, 62: 7364 -
44b
Brandt P.Hedberg C.Lawonn K.Pinho P.Andersson PG. Chem. Eur. J. 1999, 5: 1692 -
44c
Jimeno C.Reddy KS.Sola L.Moyano A.Pericas MA.Riera A. Org. Lett. 2000, 2: 3157 -
44d
Frantz DE.Fassler R.Carreira EM. J. Am. Chem. Soc. 1999, 121: 11245 -
44e
Dahmen S.Bräse S. J. Am. Chem. Soc. 2002, 124: 5940 -
45a
Fujihara H.Nagai K.Tomioka K. J. Am. Chem. Soc. 2000, 122: 12055 -
45b
Soeta T.Nagai K.Fujihara H.Kuriyama M.Tomioka K. J. Org. Chem. 2003, 68: 9723 -
46a
Porter JR.Traverse JF.Hoveyda AH.Snapper ML. J. Am. Chem. Soc. 2001, 123: 984 -
46b
Porter JR.Traverse JF.Hoveyda AH.Snapper ML. J. Am. Chem. Soc. 2001, 123: 10409 -
46c
Wipf P.Kendall C.Stephenson CRJ. J. Am. Chem. Soc. 2001, 123: 5122 -
46d
Wei C.Li C.-J. J. Am. Chem. Soc. 2002, 124: 5638 -
47a
Nakamura H.Nakamura K.Yamamoto Y. J. Am. Chem. Soc. 1998, 120: 4242 -
47b
Bao M.Nakamura H.Yamamoto Y. Tetrahedron Lett. 2000, 41: 131 - 48
Hayashi T.Ishigedani M. J. Am. Chem. Soc. 2000, 122: 976 - 49
Wang C.-J.Shi M. J. Org. Chem. 2003, 68: 6229 - 50
Shi M.Zhang W. Tetrahedron: Asymmetry 2003, 14: 3407 -
51a
Sato I.Kodaka R.Soai K. J. Chem. Soc., Perkin Trans. 1 2001, 2912 -
51b
Pinho P.Andersson PG. Tetrahedron 2001, 57: 1615 -
51c
Zhang H.-L.Zhang X.-M.Gong L.-Z.Mi A.-Q.Cui X.Jiang Y.-Z.Choi MCK.Chan ASC. Org. Lett. 2002, 4: 1399 -
51d
Boezio AA.Charette AB. J. Am. Chem. Soc. 2003, 125: 1692 -
51e
Boezio AA.Pytkowicz J.Cote A.Charette AB. J. Am. Chem. Soc. 2003, 125: 14260 -
51f
Cote A.Boezio AA.Charette AB. Angew. Chem. Int. Ed. 2004, 43: 6525 - 52
Shi M.Wang C.-J. Adv. Synth. Catal. 2003, 345: 971 -
53a
Ojima I. In Catalytic Asymmetric Synthesis VCH Publishers; Cambridge: 1993. -
53b
Noyori R. In Asymmetric Catalysis in Organic Synthesis John Wiley & Sons; New York: 1994. -
53c
Gawley RE.Aube J. In Principles of Asymmetric SynthesisBaldwin JE.Magnus PD. Pergamon; Oxford: 1996. -
54a
Noyori R.Kitamura M. Angew. Chem., Int. Ed. Engl. 1991, 30: 49 -
54b
Pu L.Yu H.-B. Chem. Rev. 2001, 101: 757 -
54c
Pu L. Tetrahedron 2003, 59: 9873 -
55a
Schmidt B.Seebach D. Angew. Chem., Int. Ed. Engl. 1991, 30: 1321 -
55b
Seebach D.Beck AK.Schmidt B.Wang YM. Tetrahedron 1994, 50: 4363 -
55c
Weber B.Seebach D. Tetrahedron 1994, 50: 7473 -
55d
Seebach D.Pichota A.Beck AK.Pinkerton AB.Litz T.Karjalainen J.Gramlich V. Org. Lett. 1999, 1: 55 -
55e
You J.-S.Shao M.-Y.Gau H.-M. Tetrahedron: Asymmetry 2001, 12: 2971 -
55f
Priego J.Mancheno OG.Cabrera S.Carretero JC. Chem. Commun. 2001, 2026 -
56a
Yoshioka M.Kawakita T.Ohno M. Tetrahedron Lett. 1989, 30: 1657 -
56b
Takahashi H.Kawakita T.Ohno M.Yoshioka M.Kobayashi S. Tetrahedron 1992, 48: 5691 -
56c
Cernerud M.Skrinning A.Bergere I.Moberg C. Tetrahedron: Asymmetry 1997, 8: 3437 -
56d
Qiu J.Guo C.Zhang X. J. Org. Chem. 1997, 62: 2665 -
56e
Lutz C.Knochel P. J. Org. Chem. 1997, 62: 7895 -
56f
Paquette LA.Zhou R. J. Org. Chem. 1999, 64: 7929 -
56g
Balsells J.Walsh PJ. J. Am. Chem. Soc. 2000, 122: 3250 -
57a
Schmidt B.Seebach D. Angew. Chem., Int. Ed. Engl. 1991, 30: 99 -
57b
Pritchett S.Woodmansee DH.Gantzel P.Walsh PJ. J. Am. Chem. Soc. 1998, 120: 6423 -
57c
Walsh PJ. Acc. Chem. Res. 2003, 36: 739 -
57d
Ding K.Du H.Yuan Y.Long J. Chem. Eur. J. 2004, 10: 2872 -
57e
Hatano M.Miyamoto T.Ishihara K. Adv. Synth. Catal. 2005, 347: 1561 - 58
Shi M.Sui W.-S. Chirality 2000, 12: 574 -
59a
Shi M.Sui W.-S. Tetrahedron: Asymmetry 1999, 10: 3319 -
59b
Shi M.Wu X.-F.Rong G. Chirality 2002, 14: 90 -
60a
Ojima I. In Catalytic Asymmetric Synthesis VCH Publishers; Weinheim: 1993. -
60b
Noyori R. In Asymmetric Catalysis in Organic Synthesis John Wiley & Sons; New York: 1994. -
60c
Gawley RE.Aube J. In Principles of Asymmetric SynthesisBaldwin JE.Magnus PD. Pergamon; Oxford: 1996. -
60d
Jacobsen N.Pfaltz A.Yamamoto H. In Comprehensive Asymmetric Catalysis Springer-Verlag; Berlin: 1999. - For several reviews on asymmetric allylation, see:
-
61a
Yamamoto Y.Asao N. Chem. Rev. 1993, 93: 2207 -
61b
Bach T. Angew. Chem., Int. Ed. Engl. 1994, 33: 417 -
61c
Hoveyda AH.Morken JP. Angew. Chem., Int. Ed. Engl. 1996, 35: 1262 -
62a
Furuta K.Mouri M.Yamamoto H. Synlett 1991, 561 -
62b
Ishihara K.Mouri M.Gao Q.Maruyama T.Furuta K.Yamamoto H. J. Am. Chem. Soc. 1993, 115: 11490 - 63
Marshall JA.Tang Y. Synlett 1992, 653 -
64a
Aoki S.Mikami K.Terada M.Nakai T. Tetrahedron 1993, 49: 1783 -
64b
Costa AL.Piazza MG.Tagliavini E.Trombini C.Umani-Ronchi A. J. Am. Chem. Soc. 1993, 115: 7001 -
64c
Keck GE.Tarbet KH.Geraci LS. J. Am. Chem. Soc. 1993, 115: 8467 -
64d
Keck GE.Geraci LS. Tetrahedron Lett. 1993, 34: 7827 -
64e
Keck GE.Krishnamurthy D.Grier MC. J. Org. Chem. 1993, 58: 6543 -
65a
Yanagisawa A.Nakashima H.Ishiba A.Yamamoto H. J. Am. Chem. Soc. 1996, 118: 4723 -
65b
Yanagisawa A.Matsumoto Y.Nakashima H.Asakawa K.Yamamoto H. J. Am. Chem. Soc. 1997, 119: 9319 -
65c
Yanagisawa A.Matsumoto Y.Asakawa K.Yamamoto H. J. Am. Chem. Soc. 1999, 121: 892 -
65d
Yanagisawa A.Nakashima H.Nakatsuka Y.Ishiba A.Yamamoto H. Bull. Chem. Soc. Jpn. 2001, 74: 1129 -
65e
Wadamoto M.Ozasa N.Yanagisawa A.Yamamoto H. J. Org. Chem. 2003, 68: 5593 -
66a
Denmark SE.Coe DM.Pratt NE.Griedel BD. J. Org. Chem. 1994, 59: 6161 -
66b
Denmark SE.Wynn T. J. Am. Chem. Soc. 2001, 123: 6199 -
67a
Shi M.Sui W.-S. Tetrahedron: Asymmetry 2000, 11: 773 -
67b
Wang C.-J.Shi M. Eur. J. Org. Chem. 2003, 2823 -
68a
Muller TE.Beller M. Chem. Rev. 1998, 98: 675 -
68b
Pohlki F.Doye S. Chem. Soc. Rev. 2003, 32: 104 - 69
Kim YK.Livinghouse T.Horino Y. J. Am. Chem. Soc. 2003, 125: 9560 - 70
Kim H.Lee PH.Livinghouse T. Chem. Commun. 2005, 5205 - 71
Duchateau R.van Wee CT.Meetsma A.Teubin JH. J. Am. Chem. Soc. 1993, 115: 4931 - 72
Kim J.-Y.Livinghouse T. Org. Lett. 2005, 7: 1737