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Jung, Michael E., Gervay, Jacquelyn (1989) Solvent effects in intramolecular Diels-Alder reactions of 2-furfuryl methyl fumarates: evidence for a polar transition state. Journal Of The American Chemical Society, 111 (14) 5469-5470 doi:10.1021/ja00196a065

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Reference TypeJournal (article/letter/editorial)
TitleSolvent effects in intramolecular Diels-Alder reactions of 2-furfuryl methyl fumarates: evidence for a polar transition state
JournalJournal Of The American Chemical Society
AuthorsJung, Michael E.Author
Gervay, JacquelynAuthor
Year1989 (July)Volume111
Issue14
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00196a065Search in ResearchGate
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Mindat Ref. ID1433275Long-form Identifiermindat:1:5:1433275:1
GUID0
Full ReferenceJung, Michael E., Gervay, Jacquelyn (1989) Solvent effects in intramolecular Diels-Alder reactions of 2-furfuryl methyl fumarates: evidence for a polar transition state. Journal Of The American Chemical Society, 111 (14) 5469-5470 doi:10.1021/ja00196a065
Plain TextJung, Michael E., Gervay, Jacquelyn (1989) Solvent effects in intramolecular Diels-Alder reactions of 2-furfuryl methyl fumarates: evidence for a polar transition state. Journal Of The American Chemical Society, 111 (14) 5469-5470 doi:10.1021/ja00196a065
In(1989, July) Journal Of The American Chemical Society Vol. 111 (14) American Chemical Society (ACS)

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Jung, Michael E., Gervay, Jacquelyn (1991) gem-Dialkyl effect in the intramolecular Diels-Alder reaction of 2-furfuryl methyl fumarates: the reactive rotamer effect, the enthalpic basis for acceleration, and evidence for a polar transition state. Journal Of The American Chemical Society, 113 (1) 224-232 doi:10.1021/ja00001a032
Jung, Michael E., Street, Leslie J. (1984) Synthetic studies on the avermectins: substituent effects on intramolecular Diels-Alder reactions of N-furfurylacrylamides and further reactions of the cycloadducts. Journal Of The American Chemical Society, 106 (26) 8327-8329 doi:10.1021/ja00338a071
Breslow, Ronald, Zhu, Zhaoning (1995) Quantitative Antihydrophobic Effects as Probes for Transition State Structures. 2. Diels-Alder Reactions. Journal Of The American Chemical Society, 117 (39) 9923-9924 doi:10.1021/ja00144a024
Jung, Michael E., Min, Sun-Joon (2005) Intramolecular Diels−Alder Reactions of Optically Active Allenic Ketones:  Chirality Transfer in the Preparation of Substituted Oxa-Bridged Octalones. Journal Of The American Chemical Society, 127 (31) 10834-10835 doi:10.1021/ja052771e
Dewar, Michael J. S., Pyron, R. Scott. (1970) Nature of the transition state in some Diels-Alder reactions. Journal Of The American Chemical Society, 92 (10) 3098-3103 doi:10.1021/ja00713a030
Houk, Ken N., Loncharich, Richard J., Blake, James F., Jorgensen, William L. (1989) Substituent effects and transition structures for Diels-Alder reactions of butadiene and cyclopentadiene with cyanoalkenes. Journal Of The American Chemical Society, 111 (26) 9172-9176 doi:10.1021/ja00208a006
Corey, E. J., Imwinkelried, Rene, Pikul, Stanislaw, Xiang, Yi Bin (1989) Practical enantioselective Diels-Alder and aldol reactions using a new chiral controller system. Journal Of The American Chemical Society, 111 (14) 5493-5495 doi:10.1021/ja00196a081
Jung, Michael E., Min, Sun-Joon (2005) Intramolecular Diels−Alder Reactions of Optically Active Allenic Ketones:  Chirality Transfer in the Preparation of Substituted Oxa-BridgedOctalones [J. Am. Chem. Soc.2005,127, 10834−10835]. Journal Of The American Chemical Society, 127 (46) 16338 doi:10.1021/ja059918m
Singleton, Daniel A. (1992) A [4 + 3] transition state for a [4 + 2] cycloaddition. A new secondary orbital interaction in Diels-Alder reactions. Journal Of The American Chemical Society, 114 (16) 6563-6564 doi:10.1021/ja00042a049
Jung, Michael E., Nishimura, Nobuko (1999) Stereoselective Formation of Formal Exo Diels−Alder Adducts of Silyloxydienes and Allenecarboxylates. Journal Of The American Chemical Society, 121 (14) 3529-3530 doi:10.1021/ja9841660
Bonnesen, Peter V., Puckett, Craig L., Honeychuck, Robert V., Hersh, William H. (1989) Catalysis of Diels-Alder reactions by low oxidation state transition-metal Lewis acids: fact and fiction. Journal Of The American Chemical Society, 111 (16) 6070-6081 doi:10.1021/ja00198a015
 
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