Total Synthesis of the Fumiquinazoline Alkaloids:  Solution-Phase Studies1

2000 ◽  
Vol 65 (4) ◽  
pp. 1022-1030 ◽  
Author(s):  
Haishan Wang ◽  
A. Ganesan
2017 ◽  
Vol 13 ◽  
pp. 919-924 ◽  
Author(s):  
Yuta Isoda ◽  
Norihiko Sasaki ◽  
Kei Kitamura ◽  
Shuji Takahashi ◽  
Sujit Manmode ◽  
...  

The total synthesis of TMG-chitotriomycin using an automated electrochemical synthesizer for the assembly of carbohydrate building blocks is demonstrated. We have successfully prepared a precursor of TMG-chitotriomycin, which is a structurally-pure tetrasaccharide with typical protecting groups, through the methodology of automated electrochemical solution-phase synthesis developed by us. The synthesis of structurally well-defined TMG-chitotriomycin has been accomplished in 10-steps from a disaccharide building block.


RSC Advances ◽  
2020 ◽  
Vol 10 (71) ◽  
pp. 43653-43659
Author(s):  
Laura Posada ◽  
Danilo Davyt ◽  
Gloria Serra

Versicotides A–C, natural products containig anthranilic acid and NMe-Ala, were prepared by Fmoc/SPPS and solution phase macrocyclization.


Tetrahedron ◽  
2011 ◽  
Vol 67 (35) ◽  
pp. 6633-6643 ◽  
Author(s):  
Tomoyasu Hirose ◽  
Takako Kasai ◽  
Takafumi Akimoto ◽  
Ayako Endo ◽  
Akihiro Sugawara ◽  
...  

2016 ◽  
Vol 14 (9) ◽  
pp. 2603-2607 ◽  
Author(s):  
Ruixuan R. Yu ◽  
Santosh K. Mahto ◽  
Kurt Justus ◽  
Mallory M. Alexander ◽  
Cecil J. Howard ◽  
...  

We report a hybrid solid-solution phase ligation approach that combines the efficiency of solid phase ligation with solution phase ligation in the total synthesis of modified histone proteins.


2020 ◽  
Author(s):  
Sandip Radhakisan Ugale ◽  
Somnath S Gholap

Abstract: A formal total synthesis of Balgacyclamide A as an antimalarial cynobactin of Microcystis aeruginosa (EAWAG 251) has been described. The synthesis of titled cyclamide was accomplished by the solution phase fragment synthesis using protection, deprotection and macrocylization process. Four common amino acids such as d-alanine, l-threonine, l-valine and d-allo-isoleucine, has been used for the construction of Balgacyclamide A. Including, the oxazoline and thiazole are the core structures was successfully achieved by using Burgess reagent and Hantzsch methods. The overall yield of the synthesized balgacyclamide A was found to be 2.03%, also structure was confirmed by1H-NMR, 13C-NMR and HRMS spectral data.


Sign in / Sign up

Export Citation Format

Share Document