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Synthese der diastereomeren 4-Amino- und 4-Hydroxy-3-(p-chlorphenyl)-valeriansäuren. Kristallstruktur von cis-4-(p-bromphenyl)-5-methyl-2-pyrrolidinon

✍ Scribed by Hans Bruderer; Wolf Arnold; Willy E. Oberhänsli


Publisher
John Wiley and Sons
Year
1978
Tongue
German
Weight
654 KB
Volume
61
Category
Article
ISSN
0018-019X

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✦ Synopsis


Synthesis of 4‐amino‐ and 4‐hydroxy‐3‐(p‐chlorophenyl)‐valeric acids. X‐ray structure of cis‐4‐(p‐bromophenyl)‐5‐methyl‐2‐pyrrolidinone

The syntheses of diastereomeric 4‐amino‐ and 4‐hydroxy‐3‐(p‐chlorophenyl)‐valeric acids and of their ring closure products (lactones and lactams), starting from 3‐(p‐chlorophenyl)‐4‐oxo‐valeric acid, are described. A single‐crystal X‐ray structure analysis of cis‐4‐(p‐bromophenyl)‐5‐methyl‐2‐pyrrolidinone is given. Some aspects of the biochemistry of threo‐3‐(p‐chlorophenyl)‐4‐amino‐valeric acid are presented.