Stereospecific dicobalt octacarbonyl mediated enyne cyclization for the synthesis of methyl deoxynorpentalenolactone H

Philip Magnus; Martin J. Slater; Lawrence M. Principe

doi:10.1021/jo00282a036

Stereospecific dicobalt octacarbonyl mediated enyne cyclization for the synthesis of methyl deoxynorpentalenolactone H

The Journal of Organic Chemistry ◽

10.1021/jo00282a036 ◽

1989 ◽

Vol 54 (21) ◽

pp. 5148-5153 ◽

Cited By ~ 38

Author(s):

Philip Magnus ◽

Martin J. Slater ◽

Lawrence M. Principe

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization

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Stereospecific dicobalt octacarbonyl-mediated enyne cyclization for the enantiospecific synthesis of a 6a-carbocycline analog

Journal of the American Chemical Society ◽

10.1021/ja00258a040 ◽

1987 ◽

Vol 109 (24) ◽

pp. 7495-7498 ◽

Cited By ~ 49

Author(s):

Philip Magnus ◽

Daniel P. Becker

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization ◽

Enantiospecific Synthesis

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ChemInform Abstract: Stereospecific Dicobalt Octacarbonyl-Mediated Enyne Cyclization for the Synthesis of Methyl Deoxynorpentalenolactone H.

ChemInform ◽

10.1002/chin.199013124 ◽

1990 ◽

Vol 21 (13) ◽

Author(s):

P. MAGNUS ◽

M. J. SLATER ◽

L. M. PRINCIPE

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization

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Stereospecific dicobalt octacarbonyl mediated enyne cyclization for the synthesis of the cytotoxic sesquiterpene (.+-.)-quadrone

The Journal of Organic Chemistry ◽

10.1021/jo00384a019 ◽

1987 ◽

Vol 52 (8) ◽

pp. 1483-1486 ◽

Cited By ~ 88

Author(s):

Philip Magnus ◽

Lawrence M. Principe ◽

Martin J. Slater

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization

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ChemInform Abstract: Stereospecific Dicobalt Octacarbonyl Mediated Enyne Cyclization for the Enantiospecific Synthesis of a 6a-Carbocycline Analogue.

ChemInform ◽

10.1002/chin.198811360 ◽

1988 ◽

Vol 19 (11) ◽

Author(s):

P. MAGNUS ◽

D. P. BECKER

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization ◽

Enantiospecific Synthesis

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ChemInform Abstract: Stereospecific Dicobalt Octacarbonyl Mediated Enyne Cyclization for the Synthesis of the Cytotoxic Sesquiterpene (.+-.)-Quadrone.

ChemInform ◽

10.1002/chin.198739078 ◽

1987 ◽

Vol 18 (39) ◽

Author(s):

P. MAGNUS ◽

L. M. PRINCIPE ◽

M. J. SLATER

Keyword(s):

Dicobalt Octacarbonyl ◽

Enyne Cyclization

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Preparation of quinoline derivatives from schiff base and vinyl ether catalyzed by dicobalt octacarbonyl

Tetrahedron Letters ◽

10.1016/s0040-4039(01)89721-5 ◽

1967 ◽

Vol 8 (42) ◽

pp. 4199-4200 ◽

Cited By ~ 19

Author(s):

T. Joh ◽

N. Hagihara

Keyword(s):

Schiff Base ◽

Vinyl Ether ◽

Quinoline Derivatives ◽

Dicobalt Octacarbonyl

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Thermodynamics for the hydrogenation of dicobalt octacarbonyl in supercritical carbon dioxide

Organometallics ◽

10.1021/om00038a014 ◽

1992 ◽

Vol 11 (2) ◽

pp. 585-588 ◽

Cited By ~ 37

Author(s):

J. W. Rathke ◽

R. J. Klingler ◽

T. R. Krause

Keyword(s):

Carbon Dioxide ◽

Supercritical Carbon Dioxide ◽

Dicobalt Octacarbonyl ◽

Supercritical Carbon

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ChemInform Abstract: NON-BRIDGED STRUCTURES OF DICOBALT OCTACARBONYL

Chemischer Informationsdienst ◽

10.1002/chin.197833299 ◽

1978 ◽

Vol 9 (33) ◽

Author(s):

D. L. LICHTENBERGER ◽

T. L. BROWN

Keyword(s):

Dicobalt Octacarbonyl

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Binuclear rhenium carbonyl nitrosyls related to dicobalt octacarbonyl and their decarbonylation products

Journal of Molecular Modeling ◽

10.1007/s00894-016-3028-7 ◽

2016 ◽

Vol 22 (7) ◽

Author(s):

Bing Xu ◽

Qian-Shu Li ◽

Yaoming Xie ◽

R. Bruce King

Keyword(s):

Dicobalt Octacarbonyl ◽

Rhenium Carbonyl

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Hydrogenation of Unsaturated Fatty Acid Methyl Esters by Dicobalt Octacarbonyl

Journal of Japan Oil Chemists Society ◽

10.5650/jos1956.14.16 ◽

1965 ◽

Vol 14 (1) ◽

pp. 16-19 ◽

Cited By ~ 2

Author(s):

Ikuei OGATA ◽

Akira MTSONO

Keyword(s):

Fatty Acid ◽

Unsaturated Fatty Acid ◽

Fatty Acid Methyl Esters ◽

Methyl Esters ◽

Dicobalt Octacarbonyl ◽

Acid Methyl

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