A Strategy for Macrocyclic Ring Closure and Functionalization Aimed toward Split-Pool Syntheses

1999 ◽  
Vol 121 (45) ◽  
pp. 10648-10649 ◽  
Author(s):  
Daesung Lee ◽  
Jason K. Sello ◽  
Stuart L. Schreiber
1999 ◽  
Vol 40 (44) ◽  
pp. 7757-7760 ◽  
Author(s):  
Elizabeth A. Jefferson ◽  
Eric E. Swayze

1979 ◽  
Vol 62 (8) ◽  
pp. 2673-2680 ◽  
Author(s):  
Karl H. Schulte-Elte ◽  
Arnold Hauser ◽  
G�nther Ohloff

2003 ◽  
Vol 56 (11) ◽  
pp. 1141 ◽  
Author(s):  
Ronald R. Fenton ◽  
Leonard F. Lindoy ◽  
Jason R. Price ◽  
Brian W. Skelton ◽  
Allan H. White

The synthesis of five 20-membered, N-benzylated macrocyclic ligands incorporating N4O2-donor sets and from one to three benzyl substituents for use in metal-ion recognition studies is described. The new derivatives were obtained by both benzylation of the pre-formed parent macrocycle using benzyl chloride in acetonitrile in the presence of base or, in one case, by performing macrocyclic ring closure using the appropriate N-benzylated triamine precursor by means of a bis-Schiff base condensation with the corresponding dialdehyde, followed by in situ reduction of the diamine linkages so formed. The single crystal X-ray structure of the symmetrically substituted, di-N-benzylated derivative is reported.


2018 ◽  
Vol 59 (2) ◽  
Author(s):  
P. Bhyrappa ◽  
◽  
M. Sankar ◽  
K. Karunanithi ◽  
B. Varghese ◽  
...  

2015 ◽  
Vol 19 (3) ◽  
pp. 274-281
Author(s):  
Milan Randic ◽  
Marjana Novic ◽  
Dejan Plavsic
Keyword(s):  

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