The Astounding Chemistry of a 2-Amino-1,2-dihydroisoquinoline Derivative
✍ Scribed by Toni Durst; Jürgen A. Finke; Rolf Huisgen; Robert Temme
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- German
- Weight
- 392 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0018-019X
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📜 SIMILAR VOLUMES
## Abstract A four‐component reaction for the synthesis of 1,2‐dihydroisoquinoline derivatives is described. The __Huisgen__ 1,4‐dipolar intermediate, which is produced from isoquinoline and an electron‐deficient acetylene compound **1**, reacts with H~2~O in the presence of diketene to produce 1,2
Spiro[pyrrole-3,2Ј-3(2H)-benzofuranones] 7 have been refluxing DMF, the spiro compounds yield tetrasubstituted pyrroles or compounds derived from chromenopyrroles. The synthesized by [4+2] cycloaddition of 2-arylidene-3(2H)benzofuranones with the 2-benzoyl-1,2-dihydroisoquinoline-regio-and stereoche
## Abstract For Abstract see ChemInform Abstract in Full Text.