Formation of pyridin-4(1H)-one versus 1H-azepin-4(7H)-one by treatment of 4-tert-butyldimethylsilyloxy-2-amino-1-aza-bicyclo[4.1.0]hept-3-enes with tetrabutylammonium fluoride-Reference-Cited by-同舟云学术

Formation of pyridin-4(1H)-one versus 1H-azepin-4(7H)-one by treatment of 4-tert-butyldimethylsilyloxy-2-amino-1-aza-bicyclo[4.1.0]hept-3-enes with tetrabutylammonium fluoride

Published:2007-11 Issue:45 Volume:63 Page:11167-11173
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Alves M. José,Fortes A. Gil,Costa F. Teixeira,Duarte Vera C.M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Generation and Diels-Alder reactions of t-butyl 2H-azirine-3-carboxylate

2. Diels–Alder cycloaddition of electrophilic 2H-azirines with 3-(3-(tert-butyldimethylsilyloxy)buta-1,3-dienyl)oxazolidin-2-ones. Treatment of the cycloadducts under acidic conditions

3. Synthesis of hydroxylated 1-azabicyclo[3.1.0]hexane and prolinol derivatives by stereo- and regiocontrolled Staudinger aminocyclization. Application to the nonproteinogenic amino acid (2S,3S,4S)-3-hydroxy-4-methylproline (HMP) and its enantiomer

4. Cycloadditions. XVI. Cycloaddition of 1-azirines to 1,3-diphenylisobenzofuran and rearrangement of the adducts

5. Reaction of 1-azirines with 1,3-diphenylisobenzofuran. Ring expansion to isoquinoline, dihydroisoquinoline, and azanorcarane derivatives

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