𝔖 Bobbio Scriptorium
✦   LIBER   ✦

LOSS OF THE α-AMINO GROUP IN LYSINE METABOLISM TO FORM PIPECOLIC ACID

✍ Scribed by Rothstein, Morton; Miller, Leon L.

Book ID
126450741
Publisher
American Chemical Society
Year
1954
Tongue
English
Weight
131 KB
Volume
76
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Decarbonylation of α-tertiary amino acid
Decarbonylation of α-tertiary amino acids application to the synthesis of polyhydroxylated indolizidines from D,L-pipecolic acid
✍ María J. Martín-López; Rosa Rodriguez; Francisco Bermejo 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 821 KB

The decarbonylation of the bicyclic a-tertiary carboxamido acid 11 led to the enamide 12, easily transformed into the indolizidine alkaloid 8,8a-trans-8-hydroxy-indolizidine 14. Likewise, the same process applied to the ¢t-substituted pipecolic acid derivative 5 led to the unsaturated ester 6 which