دورية أكاديمية
Synthesis and ring transformations of 1-amino-1,2,3,9a-tetrahydroimidazo[ 1,2-a]indol-2(9H)-ones
العنوان: | Synthesis and ring transformations of 1-amino-1,2,3,9a-tetrahydroimidazo[ 1,2-a]indol-2(9H)-ones |
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المؤلفون: | Solovjova, Joana, Martynaitis, Vytas, Holzer, Wolfgang, Mangelinckx, Sven, de Kimpe, Norbert, Šačkus, Algirdas |
المصدر: | Tetrahedron, Oxford : Pergamon-Elsevier science, 2006, vol. 62, iss. 14, p. 3309-3319 ; ISSN 0040-4020 |
سنة النشر: | 2006 |
المجموعة: | LAEI VL (Lithuanian Institute of Agrarian Economics Virtual Library) / LAEI VB (Lietuvos agrarinės ekonomikos institutasvirtualią biblioteką) |
مصطلحات موضوعية: | Hydrazides, Hydrazines, Structural identification, 1,2,3,9a-tetrahydroimidazo[1,2-a]indol-2(9H)-ones, Oxadiazoles |
الوصف: | Heating 1-carbamoylmethyl-2,3,3-trimethyl-3H-indolinium chloride in the presence of hydrazine bishydrate produces regioselectively the five-membered heterocycle 1-amino-1,2,3,9a-tetrahydro-9,9,9a-trimethylimidazo[1,2-a]indol-2(9H)-one. The assignment of the structure is based on extensive H-1, C-13 and N-15 NMR spectroscopic studies. No ring-chain tautomerism of the 1-amino-1,2,3,9atetrahydroimidazo[1,2-a]indol-2(9H)-one was observed to open-chain hydrazides or the corresponding six-membered 1,2,10,10a-tetrahydro[1,2,4]triazino[4,3-a]indol-3(4H)-one. Further transformations of 1-amino-1,2,3,9a-tetrahydroimidazo[1,2-a]indol-2(9H)-one were performed by treatment with aromatic aldehydes, acid chlorides and isocyanates giving access to 40 novel hydrazones, N,N'-diacylhydrazines, N-acyl-N'-carbamoylhydrazines and 1,3,4-oxadiazoles,. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
العلاقة: | http://ktu.lvb.lt/KTU:ELABAPDB2739894&prefLang=en_USTest |
الإتاحة: | https://doi.org/10.1016/j.tet.2006.01.054Test http://ktu.lvb.lt/KTU:ELABAPDB2739894&prefLang=en_USTest |
رقم الانضمام: | edsbas.5CCE0A41 |
قاعدة البيانات: | BASE |
الوصف غير متاح. |