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DOI: 10.1055/s-0029-1216935
Enantioselective Access to All-trans 5-Alkylpiperidine-3,4-diols: Application to the Asymmetric Synthesis of the 1-N-Iminosugar (+)-Isofagomine
Publication History
Publication Date:
28 August 2009 (online)
Abstract
Access to 3,4-disubstituted N-benzylprolinol derivatives is described that, after optimization of the ring-enlargement reaction conditions, could be efficiently transformed into the corresponding 3-hydroxypiperidines. This approach was applied to the asymmetric synthesis of (+)-isofagomine relying on regio- and stereoselective oxirane opening with the cyanide anion of a pivotal epoxypyrrolidine.
Key words
iminosugar - piperidine - ring enlargement - epoxide opening
- 1
Asano N.Nash RJ.Molyneux RJ.Fleet GWJ. Tetrahedron: Asymmetry 2000, 11: 1645 -
2a
Asano N. Curr. Top. Med. Chem. 2003, 3: 471 -
2b For a review on iminosugars
as potential antiviral agents see:
Greimel P.Spreitz J.Stutz AE.Wrodnigg TM. Curr. Top. Med. Chem. 2003, 3: 513 -
2c For a review on iminosugars
in anti-cancer therapy see:
Wrodnigg TM.Steiner AJ.Ueberbacher BJ. Anti-Cancer Agents Med. Chem. 2008, 8: 77 -
3a Miglitol
and type 2 diabetes mellitus see:
Scott LJ.Spencer CM. Drugs 2000, 59: 521 -
3b Miglustat and Gaucher disease
see:
Lachman RH. Drugs Today 2006, 42: 29 - 4
Norez C.Noel S.Wilke M.Bijvelds M.Jorna H.Melin P.DeJonge H.Becq F. FEBS Lett. 2006, 580: 2081 - 5 For a review see:
Ayad T.Génisson Y.Baltas M. Curr. Org. Chem. 2004, 8: 1211 -
6a
Ayad T.Génisson Y.Baltas M.Gorrichon L. Synlett 2001, 866 -
6b
Ayad T.Génisson Y.Baltas M.Gorrichon L. Chem. Commun. 2003, 582 -
6c
Ayad T.Génisson Y.Broussy S.Baltas M.Gorrichon L. Eur. J. Org. Chem. 2003, 2903 -
6d
Ayad T.Génisson Y.Baltas M. Org. Biomol. Chem. 2005, 3: 2626 - 7
Rives A.Génisson Y.Faugeroux V.Zedde C.Lepetit C.Chauvin R.Saffon N.Andrieu-Abadie N.Colié S.Levade T.Baltas M. Eur. J. Org. Chem. 2009, 2474 - 8 Part of this work has been published
as a preliminary communication:
Faugeroux V.Génisson Y.Andrieu-Abadie N.Colié S.Levade T.Baltas M. Org. Biomol. Chem. 2006, 4: 4437 -
9a
Fuson RC.Zirkle CL. J. Am. Chem. Soc. 1948, 70: 2760 -
9b
Paul R.Tchelitcheff S. Bull. Soc. Chim. Fr. 1958, 736 -
9c
Hammer CF.Heller SR.Craig JH. Tetrahedron 1972, 28: 239 -
9d
Hammer CF.Weber JD. Tetrahedron 1981, 37: 2173 -
9e
Harding KE.Burks SR. J. Org. Chem. 1984, 49: 40 -
9f
Calvez O.Chiaroni A.Langlois N. Tetrahedron Lett. 1998, 39: 9447 -
9g
Lee J.Hoang T.Lewis S.Weissman SA.Askin D.Volante RP.Reider PJ. Tetrahedron Lett. 2001, 42: 6223 -
9h
Deyine A.Deleroix J.-M.Langlois N. Heterocycles 2004, 64: 207 -
9i
Mino T.Saito A.Tanaka Y.Hasegawa S.Sato Y.Sakamoto M.Fujita T. J. Org. Chem. 2005, 70: 1937 -
9j For a review see:
Cossy J. Chem. Rec. 2005, 51: 70 -
10a
Cossy J.Dumas C.Michel P.Gomez Pardo D. Tetrahedron Lett. 1995, 36: 549 -
10b
Cossy J.Dumas C.Gomez Pardo D. Eur. J. Org. Chem. 1999, 1693 - 11
Cossy J.Dumas C.Gomez Pardo D. Bioorg. Med. Chem. Lett. 1997, 7: 1343 - 12
Cossy J.Dumas C.Gomez Pardo D. Synlett 1997, 905 - 13
Cossy J.Mirguet O.Gomez Pardo D. Synlett 2001, 1575 - 14
Déchamps I.Gomez Pardo D.Karoyan P.Cossy J. Synlett 2005, 1170 -
15a
Déchamps I.Gomez Pardo D.Cossy J. ARKIVOC 2007, (v): 38 -
15b
Déchamps I.Gomez Pardo D.Cossy J. Tetrahedron 2007, 63: 9082 -
16a
Wilken J.Kossenjans M.Saak W.Haase D.Pohl S.Martens J. Liebigs Ann./Recl. 1997, 573 -
16b
Mena M.Bonjosh J.Gomez Pardo D.Cossy J. J. Org. Chem. 2006, 71: 5930 -
17a
Cossy J.Mirguet O.Gomez Pardo D.Desmurs J.-R. Tetrahedron Lett. 2001, 42: 5705 -
17b
Cossy J.Mirguet O.Gomez Pardo D.Desmurs J.-R. Eur. J. Org. Chem. 2002, 3543 -
18a
Ouchi H.Mihara Y.Watanabe H.Takahata H. Tetrahedron Lett. 2004, 45: 7053 -
18b
Ouchi H.Mihara Y.Takahata H. J. Org. Chem. 2005, 70: 5207 -
19a
Jespersen TM.Dong W.Sierks MR.Skrydstrup T.Lundt I.Bols M. Angew. Chem., Int. Ed. Engl. 1994, 33: 1778 -
19b
Jespersen TM.Bols M.Sierks MR.Skrydstrup T. Tetrahedron 1994, 50: 13449 -
20a
Bols M. Acc. Chem. Res. 1998, 31: 1 -
20b
Lillelund VH.Jensen HH.Liang X.Bols M. Chem. Rev. 2002, 102: 515 -
20c
Zechel DL.Boraston AB.Gloster T.Boraston CM.Macdonald JM.Tilbrook DMG.Stick RV.Davies GJ. J. Am. Chem. Soc. 2003, 125: 14313 - 21
Zhu X.Sheth KA.Li S.Chang H.-H.Fan J.-Q. Angew. Chem. Int. Ed. 2005, 44: 7450 -
22a
Yu Z.Sawkar AR.Whalen LJ.Wong C.-H.Kelly JW. J. Med. Chem. 2007, 50: 94 -
22b
Steet R.Chung S.Lee W.-S.Pine CW.Do H.Kornfeld S. Biochem. Pharmacol. 2007, 73: 1376 -
23a
Ichikawa Y.Igarashi Y.Ichikawa M.Suhara Y. J. Am. Chem. Soc. 1998, 120: 3007 -
23b
Kim YJ.Ichikawa M.Ichikawa Y. J. Org. Chem. 2000, 65: 2599 -
23c
Hansen SU.Bols M. J. Chem. Soc., Perkin Trans. 1 2000, 911 -
23d
Pandey G.Kapur M. Tetrahedron Lett. 2000, 41: 8821 -
23e
Pandey G.Kapur M. Synthesis 2001, 1263 -
23f
Zhao G.Deo UC.Ganem B. Org. Lett. 2001, 3: 201 -
23g
Best WM.Macdonald JM.Skelton BW.Stick RV.Matthew D.Tilbrook G.White AH. Can. J. Chem. 2002, 80: 857 -
23h
Guanti G.Riva R. Tetrahedron Lett. 2003, 44: 357 -
23i
Pandey G.Kapur M.Khan MI.Gaikwad SM. Org. Biomol. Chem. 2003, 1: 3321 -
23j
Liu HZ.Lillelund VH.Andersch J.Liang XF.Bols M. J. Carbohydr. Chem. 2004, 23: 223 -
23k
Banfi L.Guanti G.Paradivino M.Riva R. Org. Biomol. Chem. 2005, 3: 1729 -
23l
Meloncelli PJ.Stick RV. Aust. J. Chem. 2006, 59: 827 -
23m
Panfil I.Solecka J.Chmielewski M. J. Carbohydr. Chem. 2006, 25: 673 -
23n
Goddard-Borger ED.Stick RV. Aust. J. Chem. 2007, 60: 211 -
23o
Mihara Y.Ojima H.Imahori T.Yoshimura Y.Ouchi H.Takahata H. Heterocycles 2007, 72: 633 -
23p
Imahori T.Ojima H.Tateyama H.Mihara Y.Takahata H. Tetrahedron Lett. 2008, 49: 265 -
23q
Imahori T.Ojima H.Yoshimura Y.Takahata H. Chem. Eur. J. 2008, 14: 10762 -
23r
Espeel PER.Piens K.Callewaert N.Van der Eycken J. Synlett 2008, 2321 - 24
Caron M.Sharpless KB. J. Org. Chem. 1985, 50: 1557 - 25
Konno H.Toshiro E.Hinoda N. Synthesis 2003, 2161 - 26
Lakner FJ.Hager LP. J. Org. Chem. 1996, 61: 3923 - 27
Ciaccio JA.Smrtka M.Maio WA.Rucando D. Tetrahedron Lett. 2004, 45: 7201 - 30
Sheldrick GM. Acta Crystallogr., Sect. A 1990, 46: 467
References
Crystal data for 12: C14H16N2O, M = 228.29, orthorhombic, P2 (1)2 (1)2 (1), a = 4.8314 (4) Å, b = 9.9404 (8) Å, c = 25.912 (2) Å, α = β = γ = 90˚, V = 1244.44 (18) ų, Z = 4, ρcalcd = 1.218 mg/m³, F(000) = 488, λ = 0.71073 Å, T = 173 (2) K, crystal size 0.70 × 0.10 × 0.10 mm³, 4458 reflections collected (2407 independent, R int = 0.0408), R1 [I > 2σ(I)] = 0.0510, wR2 [all data] = 0.1115, largest diff. peak and hole: 0.202 and -0.164 e˙Å-³. CCDC 722378 contains the supplementary crystallographic data for 12. It can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html [or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 (1223)336033; e-mail: deposit@ccdc.cam.ac.uk].
29Crystal data for 16: C15H19NO3, M = 261.31, monoclinic, P2 (1), a = 9.3250 (2) Å, b = 4.80970 (10) Å, c = 15.5678 (4) Å, α = γ = 90˚, β = 102.439 (2)˚, V = 681.83 (3) ų, Z = 2, ρcalcd = 1.273 mg/m³, F(000) = 280, λ = 0.71073 Å, T = 173 (2) K, crystal size 0.8 × 0.10 × 0.10 mm³, 10163 reflections collected (3246 independent, R int = 0.0214), R1 [I > 2σ(I)] = 0.0476, wR2 [all data] = 0.1289, largest diff. peak and hole: 0.252 and -0.172 e˙Å-³. CCDC 722379 contains the supplementary crystallographic data for 16. It can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html [or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 (1223)336033; e-mail: deposit@ccdc.cam.ac.uk].
31SHELXL-97, Program for Crystal Structure Refinement: Sheldrick, G. M., University of Göttingen, 1997.