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An easy route to optically active 1-substituted-1-pyridyl-methylamines by diastereoselective reduction of enantiopure N-tert-butanesulfinyl ketimines
Institution:1. Dipartimento di Chimica, Università di Sassari, via Vienna 2, I-07100 Sassari, Italy;2. Dipartimento Farmaco Chimico Tossicologico, Università di Sassari, Via Muroni 23, I-07100 Sassari, Italy;1. Department of Pharmaceutical Chemistry, College of Pharmacy, Hawler Medical University, Erbil 44001, Kurdistan Region, Iraq;2. School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Preston PR1 2HE, UK;1. MCS, Laboratory of Medicinal Chemistry & Synthesis, Institute for Advanced Chemistry of Catalonia (IQAC?CSIC), Jordi Girona 18-26, 08034 Barcelona, Spain;2. Laboratory of Molecular Neuropharmacology and Bioinformatics, Institut de Neurociències and Unitat de Bioestadística, Universitat Autònoma de Barcelona (UAB), 08193 Bellaterra, Spain;3. Nanoprobes and Nanoswitches, Institute for Bioengineering of Catalonia (IBEC), Baldiri Reixac, 08028, Barcelona, Spain;4. Network Biomedical Research Center on Mental Health (CIBERSAM), Spain;5. Department of Neurosciences, Institute of Functional Genomics, Université de Montpellier, Unité Mixte de Recherche 5302 CNRS, Montpellier, France;6. Unité de recherche U1191, INSERM, Montpellier, France;7. Network Biomedical Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Spain;8. Catalan Institution for Research and Advanced Studies (ICREA), Barcelona, Spain;1. Ru?er Bo?kovi? Institute, Bijeni?ka c. 54, Zagreb 10000, Croatia;2. Faculty of Science, University of Zagreb, Department of Chemistry, Zagreb, Croatia;3. University of Electronic Science and Technology, No. 4, Section 2, North Jianshe Road, Chengdu, China;1. College of Pharmacy and Institute for Drug Research, Yeungnam University, Gyeongsan 712-749, Republic of Korea;2. Department of Pharmacy and Institute of Pharmaceutical Science and Technology, Hanyang University, Ansan 426-791, Republic of Korea;1. Applied Organic Chemistry Department, National Research Centre, Cairo, Egypt;2. Faculty of Science and Arts, Mohail Asser, King Khalid University, Saudi Arabia;3. Organometallic and Organometalloid Chemistry Department, National Research Centre, Cairo, Egypt;4. Chemistry Department, Faculty of Science, Al-Azhar University (Boys), Cairo, Egypt;5. Department of Chemistry, College of Science, United Arab Emirates University, P.O. Box 15551, Al-Ain, United Arab Emirates;6. Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt;7. Department of Pharmacology and Toxicology, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt;8. Department of Medicinal Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt
Abstract:The reduction of enantiopure N-tert-butanesulfinyl ketimines derived from pyridyl ketones afforded the related N-tert-butanesulfinyl amines with high yields and diastereoselectivities.
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