trans-rac-2-Hexyl-1-oxo-3-(2-pyridyl)-1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid
✍ Scribed by Kandinska, Meglena I. ;Todorov, Iliya S. ;Shivachev, Boris ;Bogdanov, Milen G.
- Publisher
- International Union of Crystallography
- Year
- 2007
- Tongue
- English
- Weight
- 231 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1600-5368
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📜 SIMILAR VOLUMES
## Abstract Stereochemical course of the reaction of homophthalic anhydride and __N__‐(1‐methyl‐1__H__‐pyrrol‐2‐yl‐methylidene)‐phenethylamine was studied. Mixtures of the expected __trans__‐ and __cis__‐1,2,3,4‐tetrahydroiso‐quinoline‐4‐carboxylic acids trans‐**4** and cis‐**4** were obtained alon
## Abstract The reaction of homophthalic anhydride and __N__‐(1‐methyl‐1__H__‐pyrrol‐2‐yl‐methylidene)‐benzylamine in boiling benzene afforded as a main product the expected substituted __trans__‐1,2,3,4‐tetrahydroisoquinoline‐4‐carboxylic acid **5**. The carboxylic group of **5** was transformed i
In the natural product title compound, C 13 H 15 NO 4 , intramolecular O-HÁ Á ÁO hydrogen bonds help to establish the conformation. ## Related literature For background, see: Jiao et al. (2006); Shen et al. (2006). Experimental Crystal data C 13 H 15 NO 4 M r = 249.26 Orthorhombic, P2 1 2 1 2 1 a