ChemInform Abstract: Asymmetric Pictet—Spengler Reactions: Synthesis of 1,2,3,4-Tetrahydroisoquinoline Carboxylic Acid (Tic) Chimeras
✍ Scribed by Jan Spengler; Hartmut Schedel; Joachim Sieler; Peter J. L. M. Quaedflieg; Quirinus B. Broxterman; Alexander L. L. Duchateau; Klaus Burger
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
A new and general synthetic methodology for the preparation of functionalized 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives by a cycloaddition strategy is described. The synthesis of various enyne building blocks 12, 13, 21, and 22 containing an α-amino acid moiety using Schiff base 8
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Pictet-Spengler Condensation of N-Sulfonyl-β-phenethylamines with α-Chloro-α-phenylselenoesters. New Synthesis of 1,2,3,4-Tetrahydroisoquinoline-1-carboxylates. -Lewis acid promoted Pictet-Spengler type condensation of the tosylated β-phenethylamines (I) with α-chloro-α-seleno carboxylates (II) di