首页 | 本学科首页   官方微博 | 高级检索  
     


The aza-achmatowicz rearrangement: A route to useful building blocks for N- containing structures
Affiliation:1. CPQBA, University of Campinas, P.O. Box 6171, 13083-970 Campinas, SP, Brazil;2. GEQOB, ICEx, Federal University of Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil;3. UIC, University of Illinois at Chicago, 3320 MBRB, MC 865 Chicago, IL, USA;4. FCF, University of Campinas, P.O. Box 6029, 13083-859 Campinas, SP, Brazil;1. Department of Chemistry, Biochemistry and Environmental Protection, Faculty of Sciences, University of Novi Sad, Trg Dositeja Obradovića 3, 21000 Novi Sad, Serbia;2. Oncology Institute of Vojvodina, Put Doktora Goldmana 4, 21204, Sremska Kamenica, Serbia;3. Institute for Oncology and Radiology of Serbia, Pasterova 14, 11000 Belgrade, Serbia;4. Department of Physics, Faculty of Sciences, University of Novi Sad, Trg Dositeja Obradovića 4, 21000 Novi Sad, Serbia;1. Global Discovery Chemistry, Novartis Institutes for BioMedical Research, 250 Massachusetts Avenue, Cambridge, MA 02139, United States;2. Cardiovascular and Metabolism, Novartis Institutes for BioMedical Research, 100 Technology Square, Cambridge, MA 02139, United States;1. Department of Nephropathy, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230022, China
Abstract:N-Acyl 2-furylamines were transformed into 2-alkyl-6-methoxy-hexahydropyridin-3-ones. The rearranged products are useful building blocks for the total synthesis of alkaloids and unusual aminoacids.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号