ChemInform Abstract: Mild Oxidative Cleavage of 9-BBN-Protected Amino Acid Derivatives.

ChemInform ◽  
2015 ◽  
Vol 46 (44) ◽  
pp. no-no
Author(s):  
Tobias Ankner ◽  
Thomas Norberg ◽  
Jan Kihlberg
2015 ◽  
Vol 2015 (17) ◽  
pp. 3767-3770 ◽  
Author(s):  
Tobias Ankner ◽  
Thomas Norberg ◽  
Jan Kihlberg

1992 ◽  
Vol 45 (2) ◽  
pp. 395 ◽  
Author(s):  
CJ Easton ◽  
EW Tan ◽  
CM Ward

Derivatives of α,β-methanovaline, α,β-methanophenylalanine and β-methyl-αβmethanoalanine have been prepared by regioselective side-chain functionalization of suitably protected amino acid derivatives, followed by cyclization with either sodium hydride or 1,8-diazabicyclo[5.4.O]undec-7-ene. The approach used in this work illustrates a method for the synthesis of cyclopropyl amino acid derivatives which is complementary to existing procedures.


1994 ◽  
Vol 17 (13) ◽  
pp. 2759-2775 ◽  
Author(s):  
Gy. Szókán ◽  
Sz. Hadfi ◽  
K. Krizsán ◽  
A. Liembeck ◽  
I. Krecz ◽  
...  

2019 ◽  
Vol 6 (23) ◽  
pp. 3854-3858
Author(s):  
Shenpeng Tan ◽  
Feng Li ◽  
Soojun Park ◽  
Sanghee Kim

A base-mediated aerobic oxidative cleavage of α-amino esters involving a hydroperoxide intermediate was reported, which represents the first example of the cleavage of the α-C–N bonds of amino acid derivatives without the aid of metal catalysts.


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