Please use this identifier to cite or link to this item:
|Title:||A facile synthesis of telisatin A via microwave-promoted annulation and reformatsky reaction|
Chulabhorn Graduate Institute
Chulabhorn Research Institute
The Institute of Science and Technology for Research and Development, Mahidol University
|Citation:||Synlett. No.4 (2008), 505-508|
|Abstract:||A facile one-pot synthesis of 2,3-dioxopyrrolo[2,1-a]isoquinolines is reported involving the ring formation of aryl pyruvate derivatives with 3,4-dihydroisoquinolines under basic conditions and utilizing the Reformatsky reaction. Using microwave irradiation, the required compounds were obtained in moderate to good yields. © Georg Thieme Verlag Stuttgart.|
|Appears in Collections:||Scopus 2006-2010|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.