A synthesis of meta-terphenyl-2,4,6,2',5',2",4",6''-0, has been carried out. From iodobenzene-2,4,6-D, and 2,6-dibrorno-l,4-dinitrobenzene, the compound 2',5'-dinitro-meta-terphenyl-2,4,6,2'',4'',6''-D, is formed (Ullmann reaction). By reduction of the nitrogroups and subsequent reductive diazotizat
Synthesis and NMR study of [4,5,6,8-2H4][2.2]metacyclophane
✍ Scribed by Hirohisa Tsuzuki; Katsuhiko Kamio; Hideki Fujimoto; Keisuke Mimura; Susumu Matsumoto; Takehito Tsukinoki; Shuntaro Mataka; Tadashi Yonemitsu; Masashi Tashiro
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 332 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of [4,5,6,8‐^2^H~4~][2.2]metacyclophane (8) was achieved starting with 2,4,5,6‐tetrafluoroisophthalic acid in eight steps in 2% total yield. ^1^H{^2^H} and ^13^C{^1^H} NMR spectra of 8 showed that the deuterium atoms were introduced at the desired positions.
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## Abstract __N__‐(2‐Amino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**9**) and __N__‐(2,4‐diamino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**6**) were synthesized from __N__‐(4‐oxocyclohexyl)acetamide (**5**) as novel peptidomimetic building blocks. With similar purpose, __N__‐(6‐oxo‐5,6,7,
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