Thomas Hübsch
Professor
Molecular Genetics
Max Planck Institute for Molecular Genetics
Germany
Biography
Dr. Thomas Hübsch is currently working as a Professor in the Department of Molecular Genetics, Max Planck Institute for Molecular Genetics , Germany. His research interests includes Molecular Genetics. He /she is serving as an editorial member and reviewer of several international reputed journals. Dr. Thomas Hübsch is the member of many international affiliations. He/ She has successfully completed his Administrative responsibilities. He /she has authored of many research articles/books related to Molecular Genetics.
Research Interest
Molecular Genetics
Publications
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Interâ€and intramolecular hetero dielsâ€alder reactions, 40. Effect of high pressure on the stereoselectivity of intermolecular hetero dielsâ€alder reactions LF Tietze, T Hübsch, J Oelze, C Ott… - European Journal of …, 1992 - Wiley Online Library Abstract The hetero Diels-Alder reaction of enamino ketone 1 with the vinyl ethers 7–11 leading to the dihydropyrans 12a–e and 13a–e is studied in dichloromethane under high pressures up to 7 kbar. The kinetics is measured by on-line FT-IR spectroscopy up to 3 kbar. Cited by 24 Related articles All 2 versions Interâ€and Intramolecular Hetero Dielsâ€Alder Reactions, 36. Synthesis of Dihydropyrans by Hetero Dielsâ€Alder Reaction of Enaminones An Efficient Route to 3â€Amino Interâ€and intramolecular hetero dielsâ€alder reactions, 40. Effect of high pressure on the stereoselectivity of intermolecular hetero dielsâ€alder reactions LF Tietze, T Hübsch, J Oelze, C Ott… - European Journal of …, 1992 - Wiley Online Library Abstract The hetero Diels-Alder reaction of enamino ketone 1 with the vinyl ethers 7–11 leading to the dihydropyrans 12a–e and 13a–e is studied in dichloromethane under high pressures up to 7 kbar. The kinetics is measured by on-line FT-IR spectroscopy up to 3 kbar. Cited by 24 Related articles All 2 versions Interâ€and Intramolecular Hetero Dielsâ€Alder Reactions, 36. Synthesis of Dihydropyrans by Hetero Dielsâ€Alder Reaction of Enaminones An Efficient Route to 3â€Amino Interâ€and intramolecular hetero dielsâ€alder reactions, 40. Effect of high pressure on the stereoselectivity of intermolecular hetero dielsâ€alder reactions LF Tietze, T Hübsch, J Oelze, C Ott… - European Journal of …, 1992 - Wiley Online Library Abstract The hetero Diels-Alder reaction of enamino ketone 1 with the vinyl ethers 7–11 leading to the dihydropyrans 12a–e and 13a–e is studied in dichloromethane under high pressures up to 7 kbar. The kinetics is measured by on-line FT-IR spectroscopy up to 3 kbar. Cited by 24 Related articles All 2 versions Interâ€and Intramolecular Hetero Dielsâ€Alder Reactions, 36. Synthesis of Dihydropyrans by Hetero Dielsâ€Alder Reaction of Enaminones An Efficient Route to 3â€Amino Interâ€and intramolecular hetero dielsâ€alder reactions, 40. Effect of high pressure on the stereoselectivity of intermolecular hetero dielsâ€alder reactions LF Tietze, T Hübsch, J Oelze, C Ott… - European Journal of …, 1992 - Wiley Online Library Abstract The hetero Diels-Alder reaction of enamino ketone 1 with the vinyl ethers 7–11 leading to the dihydropyrans 12a–e and 13a–e is studied in dichloromethane under high pressures up to 7 kbar. The kinetics is measured by on-line FT-IR spectroscopy up to 3 kbar. Cited by 24 Related articles All 2 versions Interâ€and Intramolecular Hetero Dielsâ€Alder Reactions, 36. Synthesis of Dihydropyrans by Hetero Dielsâ€Alder Reaction of Enaminones An Efficient Route to 3â€Amino Sugar Derivatives
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Interâ€and intramolecular hetero dielsâ€alder reactions, 40. Effect of high pressure on the stereoselectivity of intermolecular hetero dielsâ€alder reactions
