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Herz, W., Kirby, G.W., Moore, R.E., Steglich, W., Tamm, Ch., Eds.; Springer-Verlag: Wien, New York
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Asakawa, Y. Progress in the Chemistry of Organic Natural Products; Herz, W., Kirby, G.W., Moore, R.E., Steglich, W., Tamm, Ch., Eds.; Springer-Verlag: Wien, New York, 1995; Vol. 65.
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(1995)
Progress in the Chemistry of Organic Natural Products
, vol.65
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Asakawa, Y.1
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2
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0034762914
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Sesqui- and diterpenoids from the Japanese liverwort Jungermannia infusca
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(a) Nagashima, F.; Suzuki, M.; Takaoka, S.; Asakawa, Y. Sesqui- and diterpenoids from the Japanese liverwort Jungermannia infusca. J. Nat. Prod. 2001, 64, 1309-1317.
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Nagashima, F.1
Suzuki, M.2
Takaoka, S.3
Asakawa, Y.4
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3
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0000260309
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Cuprenenol and rosulantol, new cuparane class sesquiterpene alcohols from the liverwort Jungermannia rosulans
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For the first report on the isolation of cuprenenol from Jungermannia Rosulans, see: (b) Matsuo, A.; Terada, I.; Nakayama, M.; Hayashi, S. Cuprenenol and rosulantol, new cuparane class sesquiterpene alcohols from the liverwort Jungermannia rosulans. Tetrahedron Lett. 1977, 3821-3824.
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Tetrahedron Lett.
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Matsuo, A.1
Terada, I.2
Nakayama, M.3
Hayashi, S.4
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4
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0030890992
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Sesqui- and diterpenoids from the Japanese liverwort Jungermannia hattoriana
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For the isolation of cuprenenol and neocuprenenols from Jungermannia infusca collected at different locations, see: (c) Nagashima, F.; Tanaka, H.; Takaoka, S.; Asakawa, Y. Sesqui- and diterpenoids from the Japanese liverwort Jungermannia hattoriana. Phytochemistry 1997, 45, 353-363;
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Phytochemistry
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Nagashima, F.1
Tanaka, H.2
Takaoka, S.3
Asakawa, Y.4
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5
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0031856175
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New sesqui- and diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt) Steph
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(d) Nagashima, F.; Suzuki, M.; Takaoka, S.; Asakawa, Y. New sesqui- and diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt) Steph. Chem. Pharm. Bull. 1998, 46, 1184-1185;
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Nagashima, F.1
Suzuki, M.2
Takaoka, S.3
Asakawa, Y.4
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6
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0033597995
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New acorane- and cuparane type sesqui and new Labdane and secolabdane type diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt.) Steph
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(e) Nagashima, F.; Suzuki, M.; Takaoka, S.; Asakawa, Y. New acorane- and cuparane type sesqui and new Labdane and secolabdane type diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt.) Steph. Tetrahedron 1999, 55, 9117-9132.
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Nagashima, F.1
Suzuki, M.2
Takaoka, S.3
Asakawa, Y.4
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7
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7644239542
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note
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To the best of our knowledge, there is no report in the literature on the synthesis of these nonaromatic cuparenoids infuscols A-D, cuprenenol, and neocuprenenol.
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8
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0001685085
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A simple stereoselective version of the Claisen rearrangement leading to trans trisubstituted olefinic bonds. Synthesis of squalene
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Johnson, W.S.; Werthemann, L.; Bartlett, W.R.; Brocksom, T.J.; Li, T.-t.; Faulkner, D.J.; Petersen, M.R. A simple stereoselective version of the Claisen rearrangement leading to trans trisubstituted olefinic bonds. Synthesis of squalene. J. Am. Chem. Soc. 1970, 92, 741-743.
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Johnson, W.S.1
Werthemann, L.2
Bartlett, W.R.3
Brocksom, T.J.4
Li, T.-T.5
Faulkner, D.J.6
Petersen, M.R.7
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9
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0032580376
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Recent advances in olefin metathesis and its applications in organic synthesis
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(a) Grubbs, R.H.; Chang, S. Recent advances in olefin metathesis and its applications in organic synthesis. Tetrahedron 1998, 54, 4413-4450;
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Grubbs, R.H.1
Chang, S.2
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10
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0344006321
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Olefin metathesis and beyond
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(b) Fürstner, A. Olefin metathesis and beyond. Angew. Chem., Int. Ed. 2000, 39, 3013-3043;
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Fürstner, A.1
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11
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0034746687
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The development of L2X2Ru=CHR olefin metathesis catalysts: An organometallic success story
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(c) Trnka, T.M.; Grubbs, R.H. The development of L2X2Ru=CHR olefin metathesis catalysts: An organometallic success story. Acc. Chem. Res. 2001, 34, 18-29.
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Trnka, T.M.1
Grubbs, R.H.2
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12
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0003032765
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A methodology for spirocyclopentannulation. Stereoselective total synthesis of tochuinyl acetate and dihydrotochuinyl acetate
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Srikrishna, A.; Reddy, T.J.; Kumar, P.P.; Vijaykumar, D. A methodology for spirocyclopentannulation. Stereoselective total synthesis of tochuinyl acetate and dihydrotochuinyl acetate. Synlett 1996, 67-68.
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(1996)
Synlett
, pp. 67-68
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Srikrishna, A.1
Reddy, T.J.2
Kumar, P.P.3
Vijaykumar, D.4
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13
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0000112955
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Remote double bond migration via rhodium catalysis: A novel enone transposition
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Grieco, P.A.; Nishizawa, M.; Marinovic, N.; Ehmann, W.J. Remote double bond migration via rhodium catalysis: A novel enone transposition. J. Am. Chem. Soc. 1976, 98, 7102-7104.
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Grieco, P.A.1
Nishizawa, M.2
Marinovic, N.3
Ehmann, W.J.4
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