Indoles from 2-Methylnitrobenzenes by Condensation with Formamide Acetals Followed by Reduction: 4-Benzyloxyindole

التفاصيل البيبلوغرافية
العنوان: Indoles from 2-Methylnitrobenzenes by Condensation with Formamide Acetals Followed by Reduction: 4-Benzyloxyindole
المؤلفون: Andrew D. Batcho, Willy Leimgruber
المصدر: Organic Syntheses
بيانات النشر: John Wiley & Sons, Inc., 2003.
سنة النشر: 2003
مصطلحات موضوعية: Formamide, chemistry.chemical_compound, Annulation, chemistry, Condensation, Organic chemistry, Alkylation, Pyrrolidine, Enamine
الوصف: Indoles from 2-Methylnitrobenzenes by Condensation with Formamide Acetals Followed by Reduction: 4-Benzyloxyindole intermediate: 6-benzyloxy-2-nitrotoluene intermediate: (E)-6-benzyloxy-2-nitro-β-pyrrolidinostyrene and (E)-6-benzyloxy-β-dimethylamino-2-nitrostyrene product: 4-benzyloxyindole intermediate: pyrrolidine enamine, mp 108–110° (MeOH), and N,N-dimethylenamine Keywords: alkenylation, C-alkenylation; alkylation, O-alkylation; aminomethylenation; annulation, heterocyclic-[5]; cyclization, reductive cyclization; reduction, miscellaneous
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0cce69aa4e5cd2996ee164e0ae22cf0f
https://doi.org/10.1002/0471264180.os063.28
رقم الأكسشن: edsair.doi...........0cce69aa4e5cd2996ee164e0ae22cf0f
قاعدة البيانات: OpenAIRE