Derivatives of Coumaran. VIII. Reductions in the Coumaranone Series. A New Synthesis of Dihydrotubanol

1941 ◽  
Vol 63 (8) ◽  
pp. 2134-2137 ◽  
Author(s):  
R. L. Shriner ◽  
Michael Witte
Keyword(s):  
2017 ◽  
Vol 13 ◽  
pp. 2153-2156 ◽  
Author(s):  
Shital Kumar Chattopadhyay ◽  
Suman Sil ◽  
Jyoti Prasad Mukherjee

A new synthesis of the important amino acid 2-aminosuberic acid from aspartic acid is reported. The methodology involves the alternate preparation of (S)-2-aminohept-6-enoate ester as a building block and its diversification through a cross-metathesis reaction to prepare the title compounds. The utility of the protocol is demonstrated through the preparation of three suberic acid derivatives of relevance to the design and the synthesis of peptides of biological relevance.


ChemInform ◽  
2004 ◽  
Vol 35 (8) ◽  
Author(s):  
V. A. Yanchenko ◽  
V. V. Malyshev ◽  
A. M. Demchenko ◽  
M. O. Lozinskii

1958 ◽  
Vol 80 (23) ◽  
pp. 6238-6244 ◽  
Author(s):  
William C. Francis ◽  
J. Robert Thornton ◽  
James C. Werner ◽  
T. R. Hopkins
Keyword(s):  

1973 ◽  
Vol 51 (12) ◽  
pp. 1915-1919 ◽  
Author(s):  
John R. McDermott ◽  
N. Leo Benoiton

Reaction of N-benzyloxycarbonyl derivatives of aliphatic amino acids, and threonine, aspartic, and glutamic acids whose side-chains were protected with the t-butyl group, gave the corresponding N-methylamino acid derivatives in good yields. The methionine derivative could be obtained by using only one mol of methyl iodide. Derivatives of threonine, and aspartic and glutamic acids whose side-chains were not protected could not be methylated. Analysis of the crude products of methylation in three cases showed that they contained 0–1% of racemized material.


Nature ◽  
1953 ◽  
Vol 171 (4356) ◽  
pp. 746-747
Author(s):  
P. M. BHARGAVA ◽  
S. HUSAIN ZAHEER
Keyword(s):  

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