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1
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0007538410
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Structure and stereochemistry of galbanic acid from galbanum
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Structure and stereochemistry of galbanic acid from galbanum: V. Y. Bagirov, V. I. Sheichenko, N. V. Veselovskaya, Y. E. Sklyar, A. A. Savina, I. Kir'yanova, Khim. Prir. Soedin. 1980, 16, 620-623.
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Bagirov, V.Y.1
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Savina, A.A.5
Kir'Yanova, I.6
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2
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0000638706
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[8], named this compound marnerai (and its corresponding alcohol marnerol) in recognition of Marner's pioneering work on iridais. Marnerai has never been isolated but was hypothesized to be the first carbocyclic precursor in the biosynthesis of iridals; a
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[8], named this compound marnerai (and its corresponding alcohol marnerol) in recognition of Marner's pioneering work on iridais. Marnerai has never been isolated but was hypothesized to be the first carbocyclic precursor in the biosynthesis of iridals; a) F.-J. Marner, W. Krick, B. Gellrich, L. Jaenicke, J. Org. Chem. 1982, 47, 2531-2538;
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Marner, F.-J.1
Krick, W.2
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5
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51649117595
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A. Corbu, M. Perez, M. Aquino, P. Retailleau, S. Arseniyadis, Org. Lett. 2008, 10, 2853-2856.
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Org. Lett.
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Corbu, A.1
Perez, M.2
Aquino, M.3
Retailleau, P.4
Arseniyadis, S.5
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6
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0028010457
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Isolation from asafetida and biogenetic derivation: a
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Isolation from asafetida and biogenetic derivation: a) G. Appendino, S. Tagliapietra, G. Nano, J. Jakupovic, Phytochemistry 1994, 35, 183-186;
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Phytochemistry
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Appendino, G.1
Tagliapietra, S.2
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Jakupovic, J.4
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7
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33747421726
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b) G. Appendino, L. Maxia, M. Bascope, P. J. Houghton, G. Sanchez-Duffhues, E. Muñoz, O. Sterner, J. Nat. Prod. 2006, 69, 1101-1104.
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Appendino, G.1
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Muñoz, E.6
Sterner, O.7
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8
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34250401989
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T. K. Khasanov, A. I. Saidkhodzhaev, G. K. Nikonov, Chem. Nat. Compd. 1974, 10, 20-23.
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Khasanov, T.K.1
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9
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0141720171
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E. M. González-García, J. Grognux, D. Wahler, J. L. Reymond, Helv. Chim. Acta 2003, 86, 2458-2470.
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González-García, E.M.1
Grognux, J.2
Wahler, D.3
Reymond, J.L.4
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10
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0041904925
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For the revised, though erroneous, structure of galbanic acid suggested by Lee et al., see
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For the revised, though erroneous, structure of galbanic acid suggested by Lee et al., see: S. G. Lee, S. Ryu, J. W. Ahn, Bull. Korean Chem. Soc. 1998, 19, 384-386.
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Lee, S.G.1
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11
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71849086233
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A. Corbu, M. Aquino, M. Perez, Z. Gandara, S. Arseniyadis, Eur. J. Org. Chem. 2009, 6386-6392.
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Corbu, A.1
Aquino, M.2
Perez, M.3
Gandara, Z.4
Arseniyadis, S.5
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12
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0344956360
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J. Jakupovic, S. Banerjee, F. Bohlmann, R. M. King, Tetrahedron 1986, 42, 1305-1313.
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Tetrahedron
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Jakupovic, J.1
Banerjee, S.2
Bohlmann, F.3
King, R.M.4
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13
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77649227607
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With the exception of the contribution reported recently by our group there appear to have been, no prior synthetic studies.
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With the exception of the contribution reported recently by our group there appear to have been, no prior synthetic studies.
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14
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19944432832
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a) H. D. Yoo, P. A. Cremin, L. Zeng, E. Garo, C. T. Williams, C. M. Lee, M. G. Goering, M. O'Neil-Johnson, G. R. Eldridge, J. F. Hu, J. Nat. Prod. 2005, 68, 122-124;
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Yoo, H.D.1
Cremin, P.A.2
Zeng, L.3
Garo, E.4
Williams, C.T.5
Lee, C.M.6
Goering, M.G.7
O'Neil-Johnson, M.8
Eldridge, G.R.9
Hu, J.F.10
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16
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0041864168
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a) L. Finet, J. I. Candela Lena, T. Kaoudi, N. Birlirakis, S. Arseniyadis, Chem. Eur. J. 2003, 9, 3813-3820;
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Chem. Eur. J
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Finet, L.1
Candela Lena, J.I.2
Kaoudi, T.3
Birlirakis, N.4
Arseniyadis, S.5
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17
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36348986803
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b) A. Corbu, G. Gauron, J. M. Castro, M. Dakir, S. Arseniyadis, Org. Lett. 2007, 9, 4745-4748.
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Corbu, A.1
Gauron, G.2
Castro, J.M.3
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Arseniyadis, S.5
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21
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0001847186
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Eds.: M. Shibasaki, J. F. Stoddart, F. Vögtle, Wiley-VCH, Weinheim
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c) L. F. Tietze, F. Haunert, in: Stimulating Concepts in Chemistry (Eds.: M. Shibasaki, J. F. Stoddart, F. Vögtle), Wiley-VCH, Weinheim, 2000, pp. 39-64;
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Stimulating Concepts in Chemistry
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Tietze, L.F.1
Haunert, F.2
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22
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84890766709
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Eds.: L. F. Tietze, G. Brasche, K. M. Gericke, Wiley-VCH, ISBN 3-527-29060-5.
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d) Domino Reactions in Organic Synthesis (Eds.: L. F. Tietze, G. Brasche, K. M. Gericke), Wiley-VCH, 2006; ISBN 3-527-29060-5.
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(2006)
Domino Reactions in Organic Synthesis
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23
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0001597205
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For an application to the taxoid ABC diterpene core see
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a) For an application to the taxoid ABC diterpene core see: J. I. Martín Hernando, J. Quílez del Moral, M. Rico Ferreira, J. I. Candela Lena, S. Arseniyadis, Tetrahedron: Asymmetry 1999, 10, 783-797;
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Tetrahedron: Asymmetry
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Martín Hernando, J.I.1
Quílez Del Moral, J.2
Rico Ferreira, M.3
Candela Lena, J.I.4
Arseniyadis, S.5
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24
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48349107034
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For an application to the first enantioselective synthesis of iridal see
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b) For an application to the first enantioselective synthesis of iridal see: A. Corbu, M. Aquino, T. V. Pratap, P. Retailleau, S. Arseniyadis, Org. Lett. 2008, 10, 1787-1790.
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Org. Lett.
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Corbu, A.1
Aquino, M.2
Pratap, T.V.3
Retailleau, P.4
Arseniyadis, S.5
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25
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48349146350
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A. Corbu, G. Gauron, J. M. Castro, M. Dakir, S. Arseniyadis, Tetrahedron: Asymmetry 2008, 19, 1730-1743.
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Tetrahedron: Asymmetry
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Corbu, A.1
Gauron, G.2
Castro, J.M.3
Dakir, M.4
Arseniyadis, S.5
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26
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0001217258
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Several protocols were examined; all conditions failed in our hands
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W. Lehnert, Tetrahedron 1973, 29, 635-638. Several protocols were examined; all conditions failed in our hands.
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(1973)
Tetrahedron
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Lehnert, W.1
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28
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0011980555
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b) J. H. Babler, D. O. Olsen, W. H. Arnold, J. Org. Chem. 1974, 39, 1656-1658;
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Babler, J.H.1
Olsen, D.O.2
Arnold, W.H.3
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30
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77649218697
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[8] (Figure Presented)
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[8] (Figure Presented)
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31
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70349513459
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-1), with the C-3 methyl ester showing better potency than, its corresponding free (galbanic) acid
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-1), with the C-3 methyl ester showing better potency than, its corresponding free (galbanic) acid: C. L. Lee, L. C. Chiang, L. H. Cheng, C. C. Liaw, M. H. Abd El-Razek, F. R. Chang, Y. C. Wu, J. Nat. Prod. 2009, 72, 1568-1572.
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Lee, C.L.1
Chiang, L.C.2
Cheng, L.H.3
Liaw, C.C.4
Abd El-Razek, M.H.5
Chang, F.R.6
Wu, Y.C.7
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34
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77649194145
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[4]
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[4]
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