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DOI: 10.1055/s-0028-1087965
3,4-Methano-β-Proline: A Conformationally Constrained β-Amino Acid
Publikationsverlauf
Publikationsdatum:
16. März 2009 (online)
Abstract
An enantiomerically pure, conformationally constrained β-proline derivative, 3,4-methano-β-proline, was synthesized starting with a readily available bicyclic lactone by using a straightforward synthetic route.
Key words
3,4-methano-β-proline - conformationally constrained β-amino acid - enantioselective synthesis
- 1
Cheng RP.Gellman SH.DeGrado WF. Chem. Rev. 2001, 101: 3219 ; and references therein -
2a
Apella DH.Christianson LA.Klein DA.Richards MR.Powell DR.Huang X.Gellman SH.
J. Am. Chem. Soc. 1999, 121: 7574 -
2b
Apella DH.Christianson LA.Klein DA.Powell DR.Huang X.Barchi JJ.Gellman SH. Nature (London) 1997, 387: 381 -
3a
Wang X.Espinosa JF.Gellman SH. J. Am. Chem. Soc. 2000, 122: 4821 -
3b
Porter EA.Wang X.Lee H.-S.Weisblum B.Gellman SH. Nature (London) 2000, 404: 565 - 4
Apella DH.Christianson LA.Karle IL.Powell DR.Gellman SH. J. Am. Chem. Soc. 1996, 118: 13071 - 5
Huck BR.Langenhan JM.Gellman SH. Org. Lett. 1999, 1: 1717 - 6
Sandvoss LM.Carlson HA. J. Am. Chem. Soc. 2003, 125: 15855 - 7
Huck BR.Fisk JD.Guzei IA.Carlson HA.Gellman SH. J. Am. Chem. Soc. 2003, 125: 9035 - For the substituted β-prolines, see:
-
8a
Denes F.Perez-Luna A.Chemla F. J. Org. Chem. 2007, 72: 398 ; and references therein -
8b
Karlsson S.Hogberg H.-E. Eur. J. Org. Chem. 2003, 2782 -
9a
Mitsumori S.Zhang H.Cheong PH.-Y.Houk KN.Tanaka F.Barbas CF. J. Am. Chem. Soc. 2006, 128: 1040 -
9b
Zhang H.Mifsud M.Tanaka F.Barbas CF. J. Am. Chem. Soc. 2006, 128: 9630 -
9c
Zhang H.Mitsumori S.Utsumi N.Imai M.Garcia-Delgado N.Mifsud M.Albertshofer K.Cheong PH.-Y.Houk KN.Tanaka F.Barbas CF. J. Am. Chem. Soc. 2008, 130: 875 - 10
Hanessian S.Shao Z.Warrier JS. Org. Lett. 2006, 8: 4787 - For studies on methano-α-prolines, see:
-
11a
Hercouet A.Bessieres B.Corre ML. Tetrahedron: Asymmetry 1996, 7: 1267 -
11b
Tverezovsky VV.Baird MS.Bolesov IG. Tetrahedron 1997, 53: 14773 -
11c
Rammeloo T.Stevens CV.De Kimpe N. J. Org. Chem. 2002, 67: 6509 -
11d
Brackmann F.Schill H.de Meijere A. Chem. Eur. J. 2005, 11: 6593 -
11e
Brackmann F.Colombo N.Cabrele C.de Meijere A. Eur. J. Org. Chem. 2006, 4440 -
11f
Hanessian S.Azzas L. Acc. Chem. Res. 2008, 41: 1241 -
11g
Brackmann F.de Meijere A. Chem. Rev. 2007, 107: 4538 -
12a
Mori M.Kubo Y.Ban Y. Tetrahedron Lett. 1985, 26: 1519 -
12b
Yang C.-H.Shen H.-J. Tetrahedron Lett. 1993, 34: 4051 - For enantioselective synthesis of β-proline, see:
-
13a
Kim YJ.Kaiser DA.Pollard TD.Ichikawa Y. Bioorg. Med. Chem. Lett. 2000, 10: 2417 -
13b
Mazzini C.Lebreton J.Alphand V.Furtoss R. J. Org. Chem. 1997, 62: 5215 -
13c
Klein SI.Czekaj M.Molino BF.Chu V. Bioorg. Med. Chem. Lett. 1997, 7: 1773 -
13d
Thomas C.Orecher F.Gmeiner P. Synthesis 1998, 1491 -
13e
Felluga F.Pitacco G.Prodan M.Pricl S.Visintin M.Valentin E. Tetrahedron: Asymmetry 2001, 12: 3241 -
13f
Cardillo G.Gentilucci L.Tolomelli A.Calienni M.Qasem AR.Sampinato S. Org. Biomol. Chem. 2003, 1: 1498 -
13g
Stoncius A.Nahrwold M.Sewald N. Synthesis 2005, 1829 -
13h
Blanchet J.Pouliquen M.Lasne M.-C.Rouden J. Tetrahedron Lett. 2007, 48: 5727 - 14
Ok T.Jeon A.Lee J.Lim JH.Hong CS.Lee H.-S. J. Org. Chem. 2007, 72: 7390 - 15
Flaniken JM.Collins CJ.Lanz M.Singaram B. Org. Lett. 1999, 1: 799 - 16
Carlsen PHJ.Katsuki T.Martin VS.Sharpless KB. J. Org. Chem. 1981, 46: 3936 - 17
Frigerio M.Santadostino M.Sputore S.Palmisano G.
J. Org. Chem. 1995, 60: 7272 - 20
Flack HD. Acta Crystallogr., Sect. A: Fundam. Crystallogr. 1983, 39: 876 ; the Flack parameter of the crystal structure of 1 was 0.0(10), and that of ent-1 was 1.0(10)
References and Notes
HPLC Data for
Boc-(3
R
,4
R
)-Methano-β-proline
Methyl Ester
t
R = 13.622
(min), area = 100%; OJ-H, IPA-n-hexane = 5:95; flow
rate = 0.4 mL/min, 25 ˚C, λ = 220
nm.
Crystal Data for
Compound 1
C11H17NO4,
crystal size: 0.10 × 0.20 × 0.20
mm³, M
r = 227.26
g mol-¹, monoclinic, space group P21, λ = 0.71073 Å, a = 6.1437
(8) Å, b = 11.3449
(17) Å, c = 9.3146
(13) Å, α = 90, β = 104.369
(10),
γ
= 90, V = 628. 92
(15) ų, Z = 2,
ρ
calcd = 1.200
g cm-³,
µ
= 0.091 min-¹, T = 293 (2)
K,
θ
range = 3.6-33.2˚;
reflections collected: 10063, independent: 4247 (R
int = 0.037).
The structure was solved by direct methods and refined by full-matrix
least-squares on F²; R
1 = 0.0432, wR
2 = 0.1196 [ I > 2σ (I)];
maximal residual electron density: 0.12 e Å-³. CCDC
710057 contains the supplementary crystallographic data for this
structure. These data can be obtained free of charge from the Cambridge
Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
HPLC Data for
Boc-(3
R
)-β-proline
Methyl Ester
t
R = 20.621
(min), area = 100%; racemic
Boc-β-proline methyl ester, t
R = 15.985,
20.824 (min). OJ-H, IPA-n-hexane = 5:95;
flow rate = 0.4 mL/min, 25 ˚C, λ = 220
nm.