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DOI: 10.1055/s-2007-983759
[2+2] Photocycloadditions with Chiral Uracil Derivatives: Access to All Four Stereoisomers of 2-Aminocyclobutanecarboxylic Acid
Publikationsverlauf
Publikationsdatum:
03. Juli 2007 (online)
Abstract
Starting from a single, chiral, bicyclic derivative of uracil, all four stereoisomers of 2-aminocyclobutanecarboxylic acid have been prepared in enantiomerically pure form, using a synthetic sequence which begins with a key photochemical [2+2] cycloaddition reaction and includes a practical cis to trans β-amino acid isomerisation procedure.
Key words
photochemistry - heterocycles - β-amino acids - cyclobutanes - stereoselective synthesis
-
1a
Spiteller P.von Nussbaum F. In Enantioselective Synthesis of β-Amino Acids 2nd ed.:Juaristi E.Soloshonok VA. Wiley-VCH; Weinheim: 2005. p.19 -
1b
von Nussbaum F.Spiteller P. In Highlights in Bioorganic Chemistry: Methods and ApplicationsSchmuck C.Wennemers H. Wiley-VCH; Weinheim: 2004. p.63 -
2a
Arvidsson PI.Ryder NS.Weiss HM.Hook DF.Escalante J.Seebach D. Chem. Biodivers. 2005, 2: 401 -
2b
Steer DL.Lew RA.Perlmutter P.Smith AI.Aguilar M.-I. Curr. Med. Chem. 2002, 9: 811 -
2c
Schreiber JV.Frackenpohl J.Moser F.Fleishmann T.Kohler H.-PE.Seebach D. ChemBioChem 2002, 3: 424 -
3a
Beke T.Somlai C.Perczel A. J. Comput. Chem. 2006, 27: 20 -
3b
Martinek TA.Fülöp F. Eur. J. Biochem. 2003, 270: 3657 -
3c
Cheng RP.Gellman SH.DeGrado WF. Chem. Rev. 2001, 101: 3219 -
3d
Möhle K.Günther R.Thormann M.Sewald N.Hofmann H.-J. Biopolymers 1999, 50: 167 -
3e
Gademann K.Hintermann T.Schreiber JV. Curr. Med. Chem. 1999, 6: 905 - For further general reviews/essays by one of the pioneers in this fascinating field, see:
-
4a
Seebach D.Beck AK.Bierbaum DJ. Chem. Biodivers. 2004, 1: 1111 -
4b
Seebach D.Kimmerlin T.Šebesta R.Campo MA.Beck AK. Tetrahedron 2004, 60: 7455 - Recent reviews:
-
5a
Enantioselective Synthesis of β-Amino Acids
Juaristi E.Soloshonok VA. Wiley-VCH; Weinheim: 2005. 2nd ed. -
5b
Liu M.Sibi MP. Tetrahedron 2002, 58: 7991 -
5c
Abele S.Seebach D. Eur. J. Org. Chem. 2000, 1 -
5d
Abdel-Magid F.Cohen JH.Maryanoff CA. Curr. Med. Chem. 1999, 6: 955 -
5e
Juaristi E.López-Ruiz H. Curr. Med. Chem. 1999, 6: 983 -
5f
Cardillo G.Tomasini C. Chem. Soc. Rev. 1996, 117 - 6
Fülöp F. Chem. Rev. 2001, 101: 2181 -
7a
Kuhl A.Hahn MG.Dumić M.Mittendorf J. Amino Acids 2005, 29: 89 -
7b
North M. J. Peptide Sci. 2000, 6: 301 -
8a
Hetényi A.Mándity IM.Martinek TA.Tóth GK.Fülöp F. J. Am. Chem. Soc. 2005, 127: 547 -
8b
Barechi JJ.Huang X.Appella DH.Christianson L.Durell SR.Gellman SH. J. Am. Chem. Soc. 2000, 122: 2711 -
8c
Appella DH.Christianson LA.Karle IL.Powell DR.Gellman SH. J. Am. Chem. Soc. 1999, 121: 6206 -
9a
Schmitt MA.Choi SH.Guzei IA.Gellman SH. J. Am. Chem. Soc. 2005, 127: 13130 -
9b
Hayen A.Schmitt MA.Ngassa FN.Thomasson KA.Gellman SH. Angew. Chem. Int. Ed. 2004, 43: 505 -
9c
Appella DH.Christianson LA.Klein DA.Richards MR.Powell DR.Gellman SH. J. Am. Chem. Soc. 1999, 121: 7574 -
9d
Appella DH.Christianson LA.Klein DA.Huang X.Barchi JJ.Powell DR.Gellman SH. Nature 1997, 387: 381 -
10a
Porter EA.Weisblum B.Gellman SH. J. Am. Chem. Soc. 2005, 127: 11516 -
10b
Schmitt MA.Weisblum B.Gellman SH. J. Am. Chem. Soc. 2004, 126: 6848 -
10c
Raguse TL.Porter EA.Weisblum B.Gellman SH. J. Am. Chem. Soc. 2002, 124: 12774 -
10d
Porter EA.Wang X.Lee H.-S.Weisblum B.Gellman SH. Nature 2000, 404: 565 - 11
Pomerantz WC.Abbott NL.Gellman SH. J. Am. Chem. Soc. 2006, 128: 8730 - 12
Martinek TA.Tóth GK.Vass E.Hollósi M.Fülöp F. Angew. Chem. Int. Ed. 2002, 41: 1718 -
13a
De Pol S.Zorn C.Klein CD.Zerbe O.Reiser O. Angew. Chem. Int. Ed. 2004, 43: 511 -
13b
Gnad F.Reiser O. Chem. Rev. 2003, 103: 1603 -
14a
Izquierdo S.Rúa F.Sbai A.Parella T.Álvarez-Larena .Branchadell V.Ortuño RM. J. Org. Chem. 2005, 70: 7963 -
14b
Izquierdo S.Martín-Vilà M.Moglioni AG.Branchadell V.Ortuño RM. Tetrahedron: Asymmetry 2002, 13: 2403 - 15
Izquierdo S.Kogan MJ.Parella T.Moglioni AG.Branchadell V.Giralt E.Ortuño RM. J. Org. Chem. 2004, 69: 5093 - 16 Recent review:
Ortuño RM.Moglioni AG.Moltrasio GY. Curr. Org. Chem. 2005, 9: 237 - Previous syntheses and uses of substituted or related derivatives:
-
17a
Mittendorf J.Kunisch F.Matzke M.Militzer H.-C.Schmidt A.Schönfeld W. Bioorg. Med. Chem. Lett. 2003, 13: 433 -
17b
Richter LS.Andersen S. Tetrahedron Lett. 1998, 39: 8747 -
17c
Yuan P.Driscoll MR.Raymond SJ.Hansen DE.Blatchly RA. Tetrahedron Lett. 1994, 35: 6195 -
17d
Mitsudo T.-A.Zhang S.-W.Satake N.Kondo T.Watanabe Y. Tetrahedron Lett. 1992, 33: 5533 -
17e
Katagiri N.Sato H.Kaneko C. Chem. Pharm. Bull. 1990, 38: 288 -
18a
Martín-Vilà M.Muray E.Aguado GP.Alvarez-Larena A.Branchadell V.Minguillón C.Giralt E.Ortuño RM. Tetrahedron: Asymmetry 2000, 11: 3569 -
18b
Martín-Vilà M.Minguillón C.Ortuño RM. Tetrahedron: Asymmetry 1998, 9: 4291 - 19
Bolm C.Schiffers I.Atodiresei I.Hackenberger CPR. Tetrahedron: Asymmetry 2003, 14: 3455 -
20a
Kennewell PD.Matharu SS.Taylor JB.Westwood R.Sammes PG. J. Chem. Soc., Perkin Trans. 1 1982, 2563 -
20b
Cannon JG.Rege AB.Gruen TL.Long JP. J. Med. Chem. 1972, 15: 71 -
20c
Shroff CC.Stewart WS.Uhm SJ.Wheeler JW. J. Org. Chem. 1971, 36: 3356 -
21a
Gauzy C.Saby B.Pereira E.Faure S.Aitken DJ. Synlett 2006, 1394 -
21b
Aitken DJ.Gauzy C.Pereira E. Tetrahedron Lett. 2002, 43: 6177 - 22 A thermal [2+2] cycloaddition approach involving highly substituted enamines and acrylate esters was examined, with some success, over 40 years ago:
Brannock KC.Bell A.Burpitt RD.Kelly CA. J. Org. Chem. 1964, 29: 801 - 23 Constrained bicyclic β-amino acid dervatives were prepared recently via an intramolecular [2+2] photocycloaddition:
Basler B.Schuster O.Bach T. J. Org. Chem. 2005, 70: 9798 - 24 Part of this work has appeared as a preliminary communication:
Gauzy C.Pereira E.Faure S.Aitken DJ. Tetrahedron Lett. 2004, 45: 7095 - For an alternative approach, using host-guest complexation for enantioselective [2+2] photocycloadditions, see:
-
25a
Furutani A.Katayama K.Uesima Y.Ogura M.Tobe Y.Kurosawa H.Tsutsumi K.Moriomoto T.Kakiuchi K. Chirality 2006, 18: 217 -
25b
Grosch B.Bach T. CRC Handbook of Organic Photochemistry and Photobiology 2nd ed.:Lenci F.Horspool WM. CRC Press; New York: 2004. p.61.1 -
25c
Bach T.Bergmann H.Grosch B.Harms K. J. Am. Chem. Soc. 2002, 124: 7982 - 26
Sekine M. J. Org. Chem. 1989, 54: 2321 - 27
Thibon J.Latxague L.Déléris G. J. Org. Chem. 1997, 62: 4635 - 28
Ludek OR.Meier C. Eur. J. Org. Chem. 2006, 941 ; and references therein -
29a
Csuk R.Eversmann L. Tetrahedron 1998, 54: 6445 -
29b
Frieden M.Giraud M.Reese CB.Song Q. J. Chem. Soc., Perkin Trans. 1 1998, 2827 -
29c
Cruickshank KA.Jiricny J.Reese CB. Tetrahedron Lett. 1984, 25: 681 -
30a
Agami C.Cheramy S.Dechoux L.Melaimi M. Tetrahedron 2001, 57: 195 -
30b
Agami C.Cheramy S.Dechoux L.Kadouri-Puchot C. Synlett 1999, 727 -
31a
Li SS.Sun XL.Ogura H.Konda Y.Sasaki T.Toda Y.Takayanagi H.Harigaya Y. Chem. Pharm. Bull. 1995, 43: 144 -
31b
Haga N.Ishikawa I.Takayanagi H.Ogura H. Bull. Chem. Soc. Jpn. 1994, 67: 728 -
31c
Sun XL.Haga N.Ogura H.Takayanagi H. Chem. Pharm. Bull. 1994, 42: 2352 -
31d
Ishikawa I.Itoh T.Takayanagi H.Oshima J.-i.Kawahara N.Mizuno Y.Ogura H. Chem. Pharm. Bull. 1991, 39: 1922 -
31e
Wexler AJ.Balchunis RJ.Swenton JS. J. Org. Chem. 1984, 49: 2733 -
31f
Wexler AJ.Hyatt JA.Raynolds PW.Cottrell C.Swenton JS. J. Am. Chem. Soc. 1978, 100: 512 -
31g
Wexler AJ.Swenton JS. J. Am. Chem. Soc. 1976, 98: 1602 -
31h
Maleski R.Morrison H. Mol. Photochem. 1972, 4: 507 - General reviews:
-
32a
Margaretha P. In Molecular and Supramolecular Photochemistry Vol. 12:Griesbeck AG.Mattay J. Marcel Dekker; New York: 2005. p.211 -
32b
Bach T. Synthesis 1998, 683 -
32c
Crimmins MT.Reinhold TL. Org. React. 1993, 44: 297 -
33a
Tsutsumi K.Nakano H.Furutani A.Endou K.Merpuge A.Shintani T.Morimoto T.Kakiuchi K. J. Org. Chem. 2004, 69: 785 -
33b
Tsutsumi K.Endou K.Furutani A.Ikki T.Nakano H.Shintani T.Morimoto T.Kakiuchi K. Chirality 2003, 15: 504 -
33c
de March P.Figuerdo M.Font J.Raya J. Tetrahedron Lett. 1999, 40: 2205 -
33d
Tsujishima H.Nakatani K.Shimamato K.Shigeri Y.Yumoto N.Ohfune Y. Tetrahedron Lett. 1998, 39: 1193 -
33e
Alibés R.Bourdelande JL.Font J.Gregori A.Parella T. Tetrahedron 1996, 52: 1267 -
33f
Alibés R.Bourdelande JL.Font J. Tetrahedron: Asymmetry 1991, 2: 1391 -
33g
Hoffmann N.Scharf H.-D. Liebigs Ann. Chem. 1991, 1273 -
33h
Kakiuchi K.Ue M.Tsukahara H.Shimizu T.Miyao T.Tobe Y.Odaira Y.Yasuda M.Shima K. J. Am. Chem. Soc. 1989, 111: 3707 ; supplementary material -
33i
Hoffmann N.Scharf H.-D.Runsink J. Tetrahedron Lett. 1989, 30: 2637 -
33j
Meyers AI.Fleming SA. J. Am. Chem. Soc. 1986, 108: 306 -
35a
Magnus NA.Confalone PN.Storace L. Tetrahedron Lett. 2000, 41: 3015 -
35b
Davies SG.Fenwick DR.Ichihara O. Tetrahedron: Asymmetry 1997, 8: 3387 -
35c
Semple JE.Wang PC.Lysenko Z.Joullié MM. J. Am. Chem. Soc. 1980, 102: 7505 -
36a
Garcia M.Azerad R. Tetrahedron: Asymmetry 1997, 8: 85 -
36b
Ingold CK.Sako S.Thorpe JF. J. Chem. Soc. 1922, 121: 1177 - 37
Aitken DJ.Gauzy C.Pereira E. Tetrahedron Lett. 2004, 45: 2359 - 38
Davies SG.Ichihara O.Lenoir I.Walters IAS. J. Chem. Soc., Perkin Trans. 1 1994, 1411 - 39
Sabbioni G.Jones JB. J. Org. Chem. 1987, 52: 4565 - 40
Malik V.Singh P.Kumar S. Tetrahedron 2005, 61: 4009
References
Crystallographic data for (-)-13a: C14H14N2O2, M = 242.27, T = 293 K, space group P61, a = 8.3788 (4) Å, b = 8.3788 (4) Å, c = 28.4565 (17) Å, α = 90.00°, β = 90.00°, γ = 120.00°, Z = 6, V = 1730.12 (16) Å3, ρcalcd = 1.395 g/cm-3. Full crystallographic data have been deposited with the Cambridge Crystallographic Data Centre (CCDC) as supplementary publication number CCDC 626949. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK, fax: +44(1223)336033, e-mail: deposit@ccdc.cam.ac.uk.