Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2009(13): 2146-2154
DOI: 10.1055/s-0029-1216842
DOI: 10.1055/s-0029-1216842
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Efficient and General Preparation of Pyranostilbenes: First Total Synthesis of Artocarbene and Pawhuskin B
Further Information
Received
14 January 2009
Publication Date:
25 May 2009 (online)
Publication History
Publication Date:
25 May 2009 (online)
Abstract
An efficient and general synthesis providing pyranostilbenes in moderate yields has been developed. It consists of the reaction of pinosylvin with the appropriate α,β-unsaturated aldehyde catalyzed by ethylenediamine diacetate. As an application of this methodology, biologically active natural products artocarbene and pawhuskin B were synthesized by a convergent sequence from commercially available aldehydes.
Key words
heterocycles - alkenes - phenols - artocarbene - pawhuskin B
-
1a
Nicolaou KC.Pfefferkorn JA.Roecker AJ.Cao G.-Q.Barluenga S.Mitchell HJ. J. Am. Chem. Soc. 2000, 122: 9939 -
1b
Nicolaou KC.Pfefferkorn JA.Mitchell HJ.Roecker AJ.Cao G.-Q.Affleck RL.Lillig JE. J. Am. Chem. Soc. 2000, 122: 9954 -
1c
Nicolaou KC.Pfefferkorn JA.Barluenga S.Mitchell HJ.Roecker AJ.Cao G.-Q. J. Am. Chem. Soc. 2000, 122: 9968 -
2a
Atwal KS.Grover GJ.Ahmed SZ.Ferrara FN.Harper TW.Kim KS.Sleph PG.Dzwonczyk S.Russell AD.Moreland S.McCullough JR.Normandin DE. J. Med. Chem. 1993, 36: 3971 -
2b
Evans JM.Fake CS.Hamilton TC.Poyser RH.Watts EA. J. Med. Chem. 1983, 26: 1582 -
2c
Cassidy F.Evans JM.Hadley MS.Haladij AH.Leach PE.Stemp G. J. Med. Chem. 1992, 35: 1623 -
2d
Gericke R.Harting J.Lues I.Schittenhelm C. J. Med. Chem. 1991, 34: 3074 -
2e
Bergmann R.Gericke R. J. Med. Chem. 1990, 33: 492 -
2f
Atwal KS.Grover GJ.Ferrara FN.Ahmed SZ.Sleph PG.Dzwonczyk S.Normandin DE. J. Med. Chem. 1995, 38: 1966 -
2g
Elomri A.Mitaku S.Michel S.Skaltsounis A.-L.Tillequin F.Koch M.Pierré A.Guilbaud N.Léonce S.Kraus-Berthier L.Rolland Y.Atass G. J. Med. Chem. 1996, 39: 4762 -
2h
Schweizer E. E.Meeder-Nycz D. Chromenes, Chromanones, and Chromones, In The Chemistry of Heterocyclic CompoundsEllis GP. Wiley; New York: 1977. Chap. 2. -
3a
Hepworth JD. In Comprehensive Heterocyclic Chemistry Vol. 3:Katritzky AR. Pergamon; New York: 1984. p.737 -
3b
Bigi F.Chesini L.Magi R.Sartori G. J. Org. Chem. 1999, 64: 1033 -
3c
Nielsen SF.Olsen CE.Christensen SB. Tetrahedron 1997, 53: 5573 -
3d
Dorta RL.Martín A.Suárez E.Betancor C. J. Org. Chem. 1997, 62: 2273 -
3e
Henry GE.Jacobs H. Tetrahedron 2001, 57: 5335 -
3f
Nguyen VTH.Langer P. Tetrahedron Lett. 2005, 46: 815 -
3g
Trost BM.Shen HC.Dong L.Surivet J.-P.Sylvain C. J. Am. Chem. Soc. 2004, 126: 11966 -
4a
Gorham J.Tori M.Asakawa Y. The Biochemistry of the Stilbenoids Chapman & Hall; London: 1995. -
4b
He S.Wu B.Pan Y.Jiang L. J. Org. Chem. 2008, 73: 5233 -
4c
Ito T.Tanaka T.Linuma M.Iliya I.Nakaya K.Ali Z.Takahashi Y.Sawa R.Shirataki Y.Murata J.Dardaedi D. Tetrahedron 2003, 59: 5347 -
4d
Sotheeswaran S.Pasupathy V. Phytochemistry 1993, 32: 1083 -
4e
Seo E.-K.Chai H.Constant HL.Santisul T.Reutrakul V.Beecher CWW.Farnsworth NR.Cordell GA.Pezzuto JM.Kinghorn AD. J. Org. Chem. 1999, 64: 6976 -
4f
Dai J.-R.Hallockm YF.Cardellina JHII.Boyd MR. J. Nat. Prod. 1998, 61: 351 - 5
Ali MA.Kondo K.Tsuda Y. Chem. Pharm. Bull. 1992, 40: 1130 - 6
Boonlaksiri C.Onnanant W.Kongsaeree P.Kittakoop M.Tanticharoen Y.Thebtaranonth Y. Phytochemistry 2000, 54: 415 -
7a
Matsuda H.Morikawa T.Toguchida I.Park JY.Harima S.Yoshikawa M. Bioorg. Med. Chem. 2001, 9: 41 -
7b
Fang J.Lu M.Chen J.Zhu H.Yang L.Wu L.Liu J. Chem. Eur. J. 2002, 8: 4191 - 8
Zheng JB.Ramirez VD. Biochem. Biophys. Res. Commun. 1999, 261: 499 -
9a
Orsini F.Pelizzoni F.Verotta L.Aburjai T. J. Nat. Prod. 1977, 60: 1082 -
9b
Aburjai TA. Phytochemistry 2000, 55: 407 - 10
Yang LM.Lin SJ.Hsu FL.Yang TH. Bioorg. Med. Chem. Lett. 2002, 12: 1013 -
11a
Wang X.Heredia A.Song H.Zhang Z.Yu B.Davis C.Redfield R. J. Pharm. Sci. 2004, 93: 2448 -
11b
Likhitwitayawuid K.Sritularak B.Benchanak K.Lipipun V.Mathew J.Schinazi RF. Nat. Prod. Res. 2005, 19: 177 - 12
Thakkar K.Geahlen RL.Cushman M. J. Med. Chem. 1993, 36: 2950 - 13
Huang KS.Lin M.Yu LN.Kong M. Tetrahedron 2000, 56: 1321 - 14
Uenobe F.Nakamura S.Miyazawa M. Mutat. Res. 1997, 373: 197 - 15
Bokel M.Diyasena C.Gunatilaka AAL.Kraus W.Sotheeswaran S. Phytochemistry 1988, 27: 377 - 16
Oshima Y.Namao K.Kamijou A.Matsuoka S.Nakano M.Terao K.Ohizumi Y. Experimentia 1995, 51: 63 - 17
Shimizu K.Kondo R.Sakai K. Phytochemistry 1997, 45: 1297 - 18
Shimizu K.Kondo R.Sakai K. Planta Med. 2000, 66: 11 - 19
Belofsky G.French AN.Wallace DR.Dodson SL. J. Nat. Prod. 2004, 67: 26 - 20
Neighbors JD.Salnikova MS.Wiemer DF. Tetrahedron Lett. 2005, 46: 1321 - 21
Fang N.Casida J. J. Nat. Prod. 1999, 62: 205 -
22a
Lee YR.Choi JH.Yoon SH. Tetrahedron Lett. 2005, 46: 7539 -
22b
Lee YR.Lee WK.Noh SK.Lyoo WS. Synthesis 2006, 853 -
22c
Lee YR.Kim DH. Synthesis 2006, 603 -
22d
Wang X.Lee YR. Tetrahedron Lett. 2007, 48: 6275 -
22e
Wang X.Lee YR. Synthesis 2007, 3044 -
22f
Lee YR.Xia L. Synthesis 2007, 3240 -
22g
Lee YR.Kim JH. Synlett 2007, 2232 -
22h
Lee YR.Li X.Kim JH. J. Org. Chem. 2008, 73: 4313 -
22i
Lee YR.Xia L. Tetrahedron Lett. 2008, 49: 3283 -
22j
Xia L.Lee YR. Synlett 2008, 1643 -
22k
Lee YR.Hung TV. Tetrahedron 2008, 64: 7338 - 23
Hua S.-Z.Wang X.-B.Luo J.-G.Wang J.-S.Kong L.-Y. Tetrahedron Lett. 2008, 49: 5658 - 24
Smith T.Modarelli DA. Tetrahedron Lett. 2008, 49: 526