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A new approach to the dibenz [b,f] azepine and [b,f] oxepine system

โœ Scribed by Ernst D. Bergmann; I. Shahak; Z. Aisenshtat


Publisher
Elsevier Science
Year
1968
Tongue
French
Weight
110 KB
Volume
9
Category
Article
ISSN
0040-4039

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๐Ÿ“œ SIMILAR VOLUMES


Dibenz[b,f]azepines, Part 7[1]: Synthesi
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Reactions of 5-carboxamido-5H-dibenz[bflazepines (la-ld) with glyoxylic acid methylester methyl hemiacetal (GMHA) led to 5-(carboxamido-N-a-hydroxy-acetic acid methyl ester)-5Hdibenz[b,Aazepines (2a-2d). The reactions with glycols yielded the oligoethylene glycol derivatives (3,4). The new compounds

Bauhinoxepins A and B: New Antimycobacte
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## Abstract Two new antimycobacterial dibenzo[__b__,__f__]oxepins, bauhinoxepins A (=3,3,5โ€trimethylbenzo[__b__]pyrano[__g__][1]benzoxepinโ€6,11โ€diol; **1**) and B (=6โ€methoxyโ€7โ€methylโ€2โ€(3โ€methylbutโ€2โ€enyl)dibenzo[__b__,__f__]oxepineโ€1,8โ€diol; **2**), were isolated from the roots of __Bauhinia sacc

ChemInform Abstract: Synthesis of an Ant
โœ Shuji Jinno; Takaaki Okita ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 29 KB ๐Ÿ‘ 1 views

Synthesis of an Antioxidant Having a Dibenz[b,f ]oxepine Skeleton. -The synthetic title compound (VI) reveals significant difference with the physicochemical data of the natural product, indicating that the original structure has to be revised. Interestingly, the antioxidative activity of synthetic