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Billard, Thierry, Langlois, Bernard R., Essers, Michael, Haufe, Günter (2008) Use of Cyclic α,β-Unsaturated Trifluoromethyl Sulfones in Diels-Alder Reactions and Michael Additions. Collection of Czechoslovak Chemical Communications, 73. 1814-1824 doi:10.1135/cccc20081814

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Reference TypeJournal (article/letter/editorial)
TitleUse of Cyclic α,β-Unsaturated Trifluoromethyl Sulfones in Diels-Alder Reactions and Michael Additions
JournalCollection of Czechoslovak Chemical Communications
AuthorsBillard, ThierryAuthor
Langlois, Bernard R.Author
Essers, MichaelAuthor
Haufe, GünterAuthor
Year2008Volume73
PublisherInstitute of Organic Chemistry & Biochemistry
DOIdoi:10.1135/cccc20081814Search in ResearchGate
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Mindat Ref. ID4392282Long-form Identifiermindat:1:5:4392282:8
GUID0
Full ReferenceBillard, Thierry, Langlois, Bernard R., Essers, Michael, Haufe, Günter (2008) Use of Cyclic α,β-Unsaturated Trifluoromethyl Sulfones in Diels-Alder Reactions and Michael Additions. Collection of Czechoslovak Chemical Communications, 73. 1814-1824 doi:10.1135/cccc20081814
Plain TextBillard, Thierry, Langlois, Bernard R., Essers, Michael, Haufe, Günter (2008) Use of Cyclic α,β-Unsaturated Trifluoromethyl Sulfones in Diels-Alder Reactions and Michael Additions. Collection of Czechoslovak Chemical Communications, 73. 1814-1824 doi:10.1135/cccc20081814
In(2008) Collection of Czechoslovak Chemical Communications Vol. 73. Institute of Organic Chemistry & Biochemistry

See Also

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Essers, Michael, Ernet, Thomas, Haufe, Günter (2003) Enantioselective Diels–Alder reactions of α-fluorinated α,β-unsaturated carbonyl compounds. Journal of Fluorine Chemistry, 121 (2). 163-170 doi:10.1016/s0022-1139(03)00010-1
Leuger, Julia, Blond, Gaelle, Billard, Thierry, Haufe, Günter, Langlois, Bernard R. (2011) 1,4-Additions of electron-rich heterocycles onto β-perfluoroalkyl enones. Journal of Fluorine Chemistry, 132 (10). 799-803 doi:10.1016/j.jfluchem.2011.04.004
Bienvenu, Antoine, Barthelemy, Audrey, Boichut, Sarah, Marquet, Bernard, Billard, Thierry, Langlois, Bernard R. (2002) Synthesis of 4-Fluorophenols from 4-tert-Butylphenols and Fluoride Sources Under Oxidative Conditions. Collection of Czechoslovak Chemical Communications, 67. 1467-1478 doi:10.1135/cccc20021467
Kofoed, Thomas (1993) Synthesis of 3'-substituted nucleosides by Michael type addition to α,β-unsaturated aldehyde. Collection of Czechoslovak Chemical Communications, 58. 269pp. doi:10.1135/cccc1993s269
Jurášek, A., Kováč, J., Kováč, M. (1976) Preparation of tetrasubstituted α,β-unsaturated sulfones of 5-nitrofuran series. Collection of Czechoslovak Chemical Communications, 41. 3371-3377 doi:10.1135/cccc19763371
Červinka, O., Kříž, O. (1973) Asymmetric reactions. XLI. Asymmetric reduction of α,β-unsaturated ketones. Collection of Czechoslovak Chemical Communications, 38. 294-297 doi:10.1135/cccc19730294
Šebo, Ľubomír, Alföldi, Juraj, Rihs, Grety, Toma, Štefan (1996) On the Stereoselectivity of the (-)-Dimenthyl Malonate Addition to α,β-Unsaturated Ketones. Collection of Czechoslovak Chemical Communications, 61. 1805-1814 doi:10.1135/cccc19961805
Červinka, O., Kříž, O. (1968) Asymmetric reactions. XXVI. Asymmetric Diels-Alder reaction. Collection of Czechoslovak Chemical Communications, 33. 2342-2345 doi:10.1135/cccc19682342
Al-Arab, Mohammad M., Issa, Ali M. (1987) Reactions of α,β-unsaturated ketones with arylacetonitriles. Collection of Czechoslovak Chemical Communications, 52. 1021-1025 doi:10.1135/cccc19871021
Kutschy, Peter, Kristian, Pavol, Dzurilla, Milan, Kováč, Jaroslav (1980) Reactions of α,β-unsaturated acyl isothiocyanates with phenylhydrazine. Collection of Czechoslovak Chemical Communications, 45. 1692-1703 doi:10.1135/cccc19801692
Blake, Alexander J., Giunta, Daniela, Shannon, Jonathan, Solinas, Maurizio, Walzer, Francesca, Woodward, Simon (2007) In Search of New Approaches to Asymmetric Conjugate Addition: Screening Studies on the Use of [Zn(bpy*)X(R)] Reagents and α,β-Unsaturated Amide Michael Acceptors. Collection of Czechoslovak Chemical Communications, 72. 1107-1121 doi:10.1135/cccc20071107
 
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