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DOI: 10.1055/s-2003-39903
Beyond Breaking the Mirror Plane: The Desymmetrisation of Centrosymmetric Molecules as an Efficient Strategy for Asymmetric Synthesis
Publikationsverlauf
Publikationsdatum:
11. Juni 2003 (online)
Abstract
Enantioselective desymmetrisation is one of the most effective strategies for asymmetric synthesis. Typically, a meso starting material with an internal mirror plane is desymmetrised by reaction with a chiral reagent; excellent yields of products as single enantiomers may be obtained. In fact, this approach is amenable to the synthesis of compounds with any embedded improper element of symmetry (such as a centre of symmetry). This review concentrates on the strategies, which are available for the synthesis of centrosymmetric (and S 4-symmetric) molecules and describes methods for their desymmetrisation. Examples of syntheses of biologically active molecules and natural products are used.
Key words
asymmetric synthesis - desymmetrisation - internal mirror plane - natural product synthesis
-
1a
Mori Y.Yaegashi K.Furukawa H. J. Am. Chem. Soc. 1997, 119: 4557 -
1b
Rainier JD.Allwein SP.Cox JM. J. Org. Chem. 2001, 66: 1380 - 2
Nicolaou KC.Yang Z.Shi G.Gunzner JL.Agrios KA.Gartner P. Nature (London) 1998, 392: 264 -
3a
Nicolaou KC. Angew. Chem., Int. Ed. Engl. 1996, 35: 589 -
3b
Nicolaou KC.Rutjes FPJT.Theodorakis EA.Tiebes J.Sato M.Untersteller E. J. Am. Chem. Soc. 1995, 117: 10252 -
4a
Hirama M.Oishi T.Uehara H.Inoue M.Maruyama M.Oguri H.Satake M. Science 2001, 294: 1904 -
4b
Inoue M.Uehara H.Maruyama M.Hirama M. Org. Lett. 2002, 4: 4551 -
5a
Fuwa H.Kainuma N.Tachibana K.Sasaki M. J. Am. Chem. Soc. 2002, 124: 14983I -
5b
Kadota I.Takamura H.Sato K.Ohno A.Matsuda K.Yamamoto Y. J. Am. Chem. Soc. 2003, 125: 46 -
6a
Nicolaou KC.Reddy KR.Skokotas G.Sato F.Xiao X.-Y. J. Am. Chem. Soc. 1992, 114: 7935 -
6b
Nicolaou KC.Reddy KR.Skokotas G.Sato F.Xiao X.-Y.Hwang C.-K. J. Am. Chem. Soc. 1993, 115: 3558 -
6c
Morimoto M.Matsukura H.Nakata T. Tetrahedron Lett. 1996, 37: 6365 -
6d
Kadota I.Yamamoto Y. J. Org. Chem. 1998, 63: 6597 -
6e
Kadota I.Jung-Youl P.Koumura N.Pollaud G.Maksukawa Y.Yamamoto Y. Tetrahedron Lett. 1995, 36: 5777 -
7a
Hayward MM. inventors; WO patent 0102787. -
7b
Blumberg LC,Brown MF,McGlynn MA,Poss CS, andGladue RP. inventors; WO patent 0172728. - 8
Maw GN. inventors; GB patent 2374074. - 9
Iwata M,Kawano N,Kaizawa H,Takuwa T,Tsukamoto I,Seo R,Yahiro K,Kobayashi M, andTakeuchi M. inventors; WO patent 0102778. - 10
Chang KJ,Pendergast W,Biciunas KP, andWu ES.-C. inventors; US patent 20020052007. - 11
Beierlein K,Bremberg U,Caldirola P,Jenmalm Jensen A,Johansson G,Mott A,Tedenborg L, andThor M. inventors; WO patent 0100822. -
12a
Wang T,Wallace OB,Zhang Z,Meanwell NA, andBender JA. inventors; WO patent 0162255. -
12b
Wang T,Wallace OB,Zhang Z,Meanwell NA, andBender JA. inventors; US patent 2002119982. - 13
Aitcher TD.Anderson RC.Gao J.Shetty SS.Coppola GM.Stanton JL.Knorr DC.Sperbeck DM.Brand LJ.Vinluan CC.Kaplan EL.Dragland CJ.Tomaselli HC.Islam A.Lozito RJ.Liu X.Maniara WM.Fillers WS.DelGrande D.Walter RE.Mann WR. J. Med. Chem. 2000, 43: 236 -
14a
Calderon SN.RiceK KC.Rothman RB.Porreca F.Flippen-Anderson JL.Kayakiri H.Xu H.Becketts K.Smith LE.Bilsky EJ.Davis P.Horvath R. J. Med. Chem. 1997, 40: 695 -
14b
Katsura Y.Zhang X.Homma K.Rice KC.Calderon SN.Rothmann R.Yamamura HI.Davis P.Flippen-Anderson JL.Xu H.Becketts K.Flotz EJ.Porreca F. J. Med. Chem. 1997, 40: 2936 - 15
Willis MC. J. Chem Soc., Perkin Trans. 1 1999, 1765 - 16
Janetka JW.Furness MS.Zhang X.Coop A.Folk JE.Mattson MV.Jacobson AE.Rice KC.Becketts K. J. Org. Chem. 2003, 68: 3976 -
17a
Fujiwara K.Morishita H.Saki K.Murai A. Tetrahedron Lett. 2000, 41: 507 -
17b
Mori Y.Mitsuoka S.Furukawa H. Tetrahedron Lett. 2000, 41: 4161 - 18
Matsuo G.Hinou H.Koshino H.Suenaga T.Nakata T. Tetrahedron Lett. 2000, 41: 903 -
19a
Gerlach H.Oertle K.Thalmann A.Servi S. Helv. Chim. Acta 1975, 58: 2036 -
19b
Schmidt U.Gombos J.Haslinger E.Zak H. Chem. Ber. 1976, 109: 2628 -
19c
Bartlett PA.Meadows JD.Ottow E. J. Am. Chem. Soc. 1984, 106: 5304 -
19d
Lee JY.Kim BH. Tetrahedron 1996, 52: 571 - 20
Fleming I.Ghosh SK. J. Chem. Soc., Perkin Trans. 1 1998, 2733 - 21
Smith WC.Xiang L.Shen B. Antimicrob. Agents Chemother. 2000, 44: 1809 - 22
Ashton PR.Cantrill SJ.Gattuso G.Menzer S.Nepogodiev SA.Shipway AN.Stoddart JF.Williams DJ. Chem.-Eur. J. 1997, 3: 1299 - 23
Whitlock CR.Cava MP. Tetrahedron Lett. 1994, 35: 371 - 24
Williams RM.Armstrong RW.Maruyama LK.Dung J.-S.Anderson OP. J. Am. Chem. Soc. 1985, 107: 3246 - 26
Spivey AC.Andrews BI.Brown AD.Frampton CS. Chem. Commun. 1999, 2523 - 27
Hoffmann RW. Angew. Chem. Int. Ed. 2003, 42: 1096 -
29a
Holland JM.Lewis M.Nelson A. Angew. Chem. Int. Ed. 2001, 40: 4082 -
29b
Holland JM.Lewis M.Nelson A. J. Org. Chem. 2003, 68: 747 - 30
Lebsack AD.Link JT.Overman LE.Stearns BA. J. Am. Chem. Soc. 2002, 124: 9008 - 31
Overman LE.Larrow JF.Stearns BA.Vance JM. Angew. Chem. Int. Ed. 2000, 39: 213 -
32a
Dodds DR.Jones JB. J. Am. Chem. Soc. 1988, 110: 577 -
32b
Baumann P.Prelog V. Helv. Chim. Acta 1958, 1: 2379 - 33
Böhm C.Austin WF.Trauner D. Tetrahedron: Asymmetry 2003, 14: 71 - 34
Ovitt TM.Coates GW. J. Am. Chem. Soc. 1999, 121: 4072
References
Anstiss, M.; Nelson, A. unpublished observations, 2003.
28W.C. Corporation, US patent 3067201, 1955.