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        Synthesis  2011(23): 3807-3814  
DOI: 10.1055/s-0031-1289293
   DOI: 10.1055/s-0031-1289293
PAPER
© Georg Thieme Verlag
      Stuttgart ˙ New YorkEfficient Synthesis of Novel Jolkinolides and Related Derivatives Starting from Stevioside
Further Information
            
               
                  
                        
                              Received
                              11 July 2011 
                      
Publication Date:
20 October 2011 (online)
            
         
      
   Publication History
Publication Date:
20 October 2011 (online)

Abstract
Jolkinolides are naturally occurring tetracyclic diterpene from Euphorbia genus, which exhibit promising antitumor and other biological activity. Efficient syntheses of the 19-carboxy derivative of jolkinolide A and 19-hydroxyjolkinolide E have been accomplished in 13 steps with a total yield of 7.8% starting from the easily available and low-cost sweetener stevioside, and some related derivatives have also been synthesized.
Key words
jolkinolides - Euphorbiaceae - stevioside - antitumor
- 1a 
             
            Che C.-T.Zhou T.-X.Ma Q.-G.Qin G.-W.Williams I.-D.Wu H.-M.Shi Z.-S. Phytochemistry 1999, 52: 117Reference Ris Wihthout Link
- 1b 
             
            Sutthivaiyakit S.Thapsut M.Prachayasittikul V. Phytochemistry 2000, 53: 947Reference Ris Wihthout Link
- 1c 
             
            Wang Y.-B.Huang R.Wang H.-B.Jin H.-Z.Lou L.-G.Qin G.-W. J. Nat. Prod. 2006, 69: 967Reference Ris Wihthout Link
- 2a 
             
            Shi YP.He ZJ.Jia JZ. Nat. Prod. Res. Dev. 1999, 11: 85Reference Ris Wihthout Link
- 2b 
             
            Su X.-L.Lin R.-C.Wong S.-K.Tsui S.-K.Kwan S.-Y. Phytochem. Anal. 2003, 14: 40Reference Ris Wihthout Link
- 3a 
             
            Zhang DY.Shi LY.Wu XM. Chin. J. Org. Chem. 2009, 29: 188Reference Ris Wihthout Link
- 3b 
             
            Lai AR.Cambie RC.Rutledge PS.Woogate PD. Phytochemistry 1990, 29: 2239Reference Ris Wihthout Link
- 3c 
             
            Luo H.-Y.Wang A.-Q. Can. J. Physiol. Pharmacol. 2006, 84: 959Reference Ris Wihthout Link
- 3d 
             
            Yamaguchi K.Uemura D.Tsuji T.Kondo K. Biosci. Biotechnol. Biochem. 1994, 58: 1749Reference Ris Wihthout Link
- 4 
             
            Shi H.-M.Williams ID.Sung HY.Zhu H.-X.Ip NY.Min Z.-D. Planta Med. 2005, 71: 349Reference Ris Wihthout Link
- 5a 
             
            Yan S.-S.Li Y.Wang Y.Shen S.-S.Gu Y.Wang H.-B.Qin G.-W.Yu Q. Mol. Cancer Ther. 2008, 7: 1523Reference Ris Wihthout Link
- 5b 
             
            Wang Y.Ma X.Yan S.Shen S.Zhu H.Gu Y.Wang H.Qin G.Yu Q. Cancer. Res. 2009, 69: 7302Reference Ris Wihthout Link
- 6 
             
            Katsumura S.Kimura A.Isoe S. Tetrahedron 1989, 45: 1337Reference Ris Wihthout Link
- 7 
             
            Ogawa T.Nozaki M.Matsui M. Tetrahedron 1980, 36: 2641Reference Ris Wihthout Link
- 8a 
             
            Cui Y.-M.Yasutomi E.Otani Y.Yoshinaga T.Ido K.Sawada K.Ohwada T. Bioorg. Med. Chem. Lett. 2008, 18: 5197Reference Ris Wihthout Link
- 8b 
             
            Singh SB.Ondeyka JG.Liu W.Chen S.Chen TS.Li X.Bouffard A.Dropinski J.Jones AB.McCormick S.Hayes N.Wang J.Sharma N.MacNaul K.Hernandez M.Chao Y.-S.Baffic J.Lam M.-H.Burton C.Sparrow CP.Menke JG. Bioorg. Med. Chem. Lett. 2005, 15: 2824Reference Ris Wihthout Link
- 9 
             
            Blay G.Garcia B.Molina E.Pedro JR. Tetrahedron 2007, 63: 9621Reference Ris Wihthout Link
- 10 
             
            Terai T.Ren H.Mori G.Yashihito Y.Hayashi T. Chem. Pharm. Bull. 2002, 50: 1007Reference Ris Wihthout Link
- 11 
             
            Bailey PS. Chem. Rev. 1958, 58: 925Reference Ris Wihthout Link
- 12a 
             
            McMurry JE.Blaszczak LC. J. Org. Chem. 1974, 39: 2217Reference Ris Wihthout Link
- 12b 
             
            Schultz AG.Wang A. J. Org. Chem. 1996, 61: 4857Reference Ris Wihthout Link
- 13 
             
            Wasserman HH.Ives JL. J. Am. Chem. Soc. 1976, 98: 7868Reference Ris Wihthout Link
- 14a 
             
            Jiang B.Shi H.-P.Tian W.-S.Zhou W.-S. Tetrahedron 2008, 64: 469Reference Ris Wihthout Link
- 14b 
             
            Furber M.Mander LN.Patrick GL. J. Org. Chem. 1990, 55: 4860Reference Ris Wihthout Link
- 15a 
             
            Rubottom GM.Vazquez MA.Pelegrina DR. Tetrahedron Lett. 1974, 15: 4319Reference Ris Wihthout Link
- 15b 
             
            Rubottom GM.Gruber JM.Boeckman RK.Ramaiah M.Medwid JB. Tetrahedron Lett. 1978, 19: 4603Reference Ris Wihthout Link
- 16 
             
            Mosettig E.Beglinger U.Dolder F.Lichti H.Quitt P.Waters JA. J. Am. Chem. Soc. 1963, 85: 2305Reference Ris Wihthout Link
- 17 
             
            Miyake T.Kigoshi H.Akita H. Tetrahedron: Asymmetry 2007, 18: 2915Reference Ris Wihthout Link
- 18 
             
            Lai G.-F.Wang X.-Y.Wang Y.-F.Cao J.-X.Luo S.-D.Ju P. Helv. Chim. Acta 2009, 92: 470Reference Ris Wihthout Link
 
    