ε-Amino acids based on bicyclic skeleton: bicyclo [3.3. 0] octane-5-amino-1-carboxylic acids
SJ Yeo, KS Jeong, H Han, J Kim, N Jeong
Index: Yeo, Sung Jin; Jeong, Kyung Seok; Han, Hogyu; Kim, Jaheon; Jeong, Nakcheol Tetrahedron Letters, 2006 , vol. 47, # 41 p. 7389 - 7393
Full Text: HTML
Citation Number: 8
Abstract
Tsc-protected ε-amino acids, bicyclo[3.3.0]octane-5-amino-1-carboxylic acids (1), ready to use in the solid-phase synthesis, are prepared from 4,4-diethylcarboxylic bicyclo[3.3.0]oct-2-enone (3), which is available in bulk from 2 through the catalytic Pauson-Khand reaction. ... Tsc-protected ε-amino acids, bicyclo[3.3.0]octane-5-amino-1-carboxylic acids (1), are prepared from 4,4-diethylcarboxylic bicyclo[3.3.0]oct-2-enone (3), which is available in bulk from 2 through the catalytic ...
Related Articles:
[Benedetti, Erica; Simonneau, Antoine; Hours, Alexandra; Amouri, Hani; Penoni, Andrea; Palmisano, Giovanni; Malacria, Max; Goddard, Jean-Philippe; Fensterbank, Louis Advanced Synthesis and Catalysis, 2011 , vol. 353, # 11-12 p. 1908 - 1912]
[Asano, Keisuke; Uesugi, Yuki; Yoshida, Jun-Ichi Organic Letters, 2013 , vol. 15, # 10 p. 2398 - 2401]
[Schulte et al. Archiv der Pharmazie (Weinheim, Germany), 1958 , vol. 291, p. 227,236]
[Chatani, Naoto; Takeyasu, Takumi; Horiuchi, Nobuhiko; Hanafusa, Terukiyo Journal of Organic Chemistry, 1988 , vol. 53, # 15 p. 3539 - 3548]