ChemInform Abstract: Oxidative Decarboxylation of Cyclic Amino Acids and Dehydrogenation of Cyclic Secondary Amines with Iodosobenzene.

ChemInform ◽  
1989 ◽  
Vol 20 (26) ◽  
Author(s):  
M. OCHIAI ◽  
M. INENAGA ◽  
Y. NAGAO ◽  
R. M. MORIARTY ◽  
R. K. VAID ◽  
...  
1988 ◽  
Vol 29 (52) ◽  
pp. 6917-6920 ◽  
Author(s):  
Masahito Ochiai ◽  
Minako Inenaga ◽  
Yoshimitsu Nagao ◽  
Robert M. Moriarty ◽  
Radhe K Vaid ◽  
...  

Tetrahedron ◽  
2004 ◽  
Vol 60 (3) ◽  
pp. 717-728 ◽  
Author(s):  
Richard C Lloyd ◽  
Michael C Lloyd ◽  
Mark E.B Smith ◽  
Karen E Holt ◽  
Jonathan P Swift ◽  
...  

2021 ◽  
Author(s):  
Zhiqiang Pan ◽  
Fengchi Hu ◽  
Di Jiang ◽  
Yuchang Liu ◽  
Chengfeng Xia

The photoexcited enamines derived from α-amino acids could undergo an oxidative decarboxylation followed by a Chichibabin cyclization to afford highly substituted pyridiniums.


Polyhedron ◽  
2015 ◽  
Vol 89 ◽  
pp. 91-95 ◽  
Author(s):  
Dóra Lakk-Bogáth ◽  
Miklós Harasztia ◽  
Róbert Csonka ◽  
Gábor Speier ◽  
József Kaizer

Author(s):  
Andreas A Grauer ◽  
Burkhard König

Cα-Tetrasubstituted α-amino acids are important building blocks for the synthesis of peptidemimetics with stabilized secondary structure, because of their ability to rigidify the peptide backbone. Recently our group reported a new class of cyclic Cα-tetrasubstituted tetrahydrofuran α-amino acids prepared from methionine and aromatic aldehydes. We now report the extension of this methodology to aliphatic aldehydes. Although such aldehydes are prone to give aldol products under the reaction conditions used, we were able to obtain the target cyclic amino acids in low to moderate yields and in some cases with good diastereoselectivity.


2007 ◽  
Vol 11 (07) ◽  
pp. 537-546 ◽  
Author(s):  
Clifford C. Leznoff ◽  
Annette Hiebert ◽  
Sibel Ok

Primary amines, secondary amines and tertiary butyl esters of amino acids are used as nucleophiles with zinc(II) hexadecafluorophthalocyanine to provide mixtures of mono and disubstituted fluorinated phthalocyanines under mild conditions, or polyaminosubstituted phthalocyanines when using the amines as solvents. Diamines give cyclic substituted phthalocyanines, binuclear or trinuclear phthalocyanines or mixtures of both types, depending on the chain length or structure of the diamine.


1984 ◽  
Vol 20 (5) ◽  
pp. 576-576
Author(s):  
A. V. Eremeev ◽  
F. D. Polyak ◽  
�. �. Liepin'sh

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