Faculty Opinions recommendation of Large scale preparation of silicon-functionalized SynPhase Polystyrene lanterns for solid-phase synthesis.

Author(s):  
Anthony Czarnik
Tetrahedron ◽  
1994 ◽  
Vol 50 (8) ◽  
pp. 2617-2622 ◽  
Author(s):  
F.Xavier Montserrat ◽  
Anna Grandas ◽  
Ramon Eritja ◽  
Enrique Pedroso

2015 ◽  
Vol 6 (3) ◽  
pp. 1645-1649 ◽  
Author(s):  
Deborah Crawford ◽  
José Casaban ◽  
Robert Haydon ◽  
Nicola Giri ◽  
Tony McNally ◽  
...  

Continuous flow mechanochemical and melt-phase synthesis at kg h−1 rates from solid reagents and either no solvent, or only minimal solvent, is reported.


Small ◽  
2011 ◽  
Vol 7 (7) ◽  
pp. 957-964 ◽  
Author(s):  
Sanjay K. Apte ◽  
Sunil N. Garaje ◽  
Gurudas P. Mane ◽  
Ajayan Vinu ◽  
Sonali D. Naik ◽  
...  

2021 ◽  
Vol 47 (6) ◽  
pp. 1241-1248
Author(s):  
D. V. Avdeev ◽  
M. V. Ovchinnikov ◽  
Y. S. Dudkina ◽  
A. S. Molokoedov ◽  
A. A. Azmuko ◽  
...  

Abstract This work is devoted to the large-scale solid-phase synthesis (SPS) of Atosiban, Mpa1-D-Tyr(OEt)-Ile-Thr-Asn-Cys6-Pro-Orn-Gly-NH2 cyclic 1,6 disulfide, the only clinically used oxytocin receptor antagonist. The conditions have been selected for the closure of the disulfide bond (S–S) in the Atosiban molecule both in the solution and solid phase with the minimal formation of by-products. A comparative assessment of the formation of the S–S bond was carried out under various conditions. The formation of by-products during the closure of the disulfide bond has been studied both in solution and on the polymer support. The developed technique allows for the synthesis of Atosiban on an enlarged scale (10–20 mmol) involving the cyclization of a protected intermediate with the formation of the S–S bond during solid-phase synthesis with the minimal formation of by-products.


2020 ◽  
Vol 44 (23) ◽  
pp. 9634-9646 ◽  
Author(s):  
Sonali D. Naik ◽  
Sanjay K. Apte ◽  
Sunil N. Garaje ◽  
Yogesh A. Sethi ◽  
Manish D. Shinde ◽  
...  

Nanostructured CdIn2S4 and ZnIn2S4 with unique morphologies can be synthesized using this method which is simple and easy to operate.


Peptides ◽  
1988 ◽  
pp. 204-207
Author(s):  
Martin S. Edelstein ◽  
John L. Hughes ◽  
Pradip K. Bhatnagar ◽  
Jonathan E. Foster ◽  
Kenneth D. Tubman ◽  
...  

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