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4
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0002202416
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112-118, 168-172
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Dragutan V., Dragutan I., Balaban A.T. Platinum Metals Rev. 44:2000;58-66., 112-118, 168-172.
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Dragutan, V.1
Dragutan, I.2
Balaban, A.T.3
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12
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0037122126
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Arisawa M., Terada Y., Nakagawa M., Nishida A. Angew. Chem., Int. Ed. 41:2002;4732-4734.
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Arisawa, M.1
Terada, Y.2
Nakagawa, M.3
Nishida, A.4
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17
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85031135820
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6-Ring Systems with Two O-Atoms, 1,4-Dioxins and Annulated Derivatives
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Schaumann E. Stuttgart: Georg Thieme Verlag
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Palar H., Angerhöfer D. 6-Ring Systems with Two O-Atoms, 1,4-Dioxins and Annulated Derivatives. Schaumann E. Houben-Weyl Methods of Organic Chemistry, Hetarenes IV, Six-Membered and Larger Hetero-Rings with Maximum Unsaturation. E9a:1997;3-38 Georg Thieme Verlag, Stuttgart.
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Houben-Weyl Methods of Organic Chemistry, Hetarenes IV, Six-Membered and Larger Hetero-Rings with Maximum Unsaturation
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, pp. 3-38
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Palar, H.1
Angerhöfer, D.2
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20
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85031134674
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Some of this work was taken from the MSc dissertation of Mr. E. L. Ngidi.
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Some of this work was taken from the MSc dissertation of Mr. E. L. Ngidi.
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21
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85031134458
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3, 75 MHz): δ 96.0; 114.2; 125.3; 126.7; 130.3; 146.5; 148.3.
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3, 75 MHz): δ 96.0; 114.2; 125.3; 126.7; 130.3; 146.5; 148.3.
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22
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85031143571
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All new compounds were fully characterized and gave satisfactory spectroscopic data.
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All new compounds were fully characterized and gave satisfactory spectroscopic data.
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23
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0034335520
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Krompiec S., Kuźnik N., Bieg T., Adamus B., Majnusz J., Grymel M. Pol. J. Chem. 74:2000;1197-1200.
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Pol. J. Chem.
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, pp. 1197-1200
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Krompiec, S.1
Kuźnik, N.2
Bieg, T.3
Adamus, B.4
Majnusz, J.5
Grymel, M.6
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27
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85031139895
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3 to facilitate comparison with literature data.
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3 to facilitate comparison with literature data.
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32
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0033603294
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Ackermann L., Fürstner A., Weskamp T., Kohl F.J., Herrmann W.A. Tetrahedron Lett. 40:1999;4787-4790.
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Ackermann, L.1
Fürstner, A.2
Weskamp, T.3
Kohl, F.J.4
Herrmann, W.A.5
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39
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85031134400
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3, 75 MHz): δ 20.3; 115.8; 116.8; 124.3; 126.6; 126.8; 134.0; 140.3; 142.2.
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3, 75 MHz): δ 20.3; 115.8; 116.8; 124.3; 126.6; 126.8; 134.0; 140.3; 142.2.
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41
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84903931024
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Furans, benzofurans, isobenzofurans, and their reduced forms
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M. Sainsbury. Amsterdam: Elsevier Science
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Hurst D.T. Furans, benzofurans, isobenzofurans, and their reduced forms. Sainsbury M. Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds, Vol IV: Heterocyclic Compounds, Pt A: Three, Four and Five Membered Monoheterocyclic Compounds. 1997;283-335 Elsevier Science, Amsterdam.
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Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds, Vol IV: Heterocyclic Compounds, Pt A: Three, Four and Five Membered Monoheterocyclic Compounds
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Hurst, D.T.1
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42
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0038401068
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On the day of submission of this manuscript we became aware of a related, recent communication by the De Kimpe group that describes the synthesis of a range of substituted coumarins. The key step described in this paper is the RCM of an isomerized 1-propenylbenzene with an α,β-unsaturated ester to afford the coumarin skeleton:
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On the day of submission of this manuscript we became aware of a related, recent communication by the De Kimpe group that describes the synthesis of a range of substituted coumarins. The key step described in this paper is the RCM of an isomerized 1-propenylbenzene with an α,β-unsaturated ester to afford the coumarin skeleton: Nguyen Van T., Debenedetti S., De Kimpe N. Tetrahedron Lett. 44:2003;4199-4201.
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(2003)
Tetrahedron Lett.
, vol.44
, pp. 4199-4201
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Nguyen Van, T.1
Debenedetti, S.2
De Kimpe, N.3
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