scholarly journals Zinc Dust Mediated Peptide Synthesis from Fmoc-Amino Acid Chlorides and Amino Acid Hydrochlorides

Synfacts ◽  
2021 ◽  
Vol 17 (08) ◽  
pp. 0951
1998 ◽  
Vol 39 (52) ◽  
pp. 9769-9772 ◽  
Author(s):  
Hosahydya N. Gopi ◽  
Vommina V. Suresh Babu
Keyword(s):  

2007 ◽  
Vol 72 (24) ◽  
pp. 9360-9363 ◽  
Author(s):  
Subramanyam J Tantry ◽  
Rao Venkataramanarao ◽  
Gundala Chennakrishnareddy ◽  
Vommina Venkata Sureshbabu

2020 ◽  
Vol 17 (8) ◽  
pp. 645-653
Author(s):  
Zetryana Puteri Tachrim ◽  
Kazuhiro Oida ◽  
Fumina Ohashi ◽  
Natsumi Kurokawa ◽  
Lei Wang ◽  
...  

α-Amino acid chlorides are reactive coupling agents in amide (peptide) formation. The Vilsmeier reagent ((chloromethylene)dimethylammonium chloride) offers a convenient way to prepare α-amino acid chlorides for peptide synthesis. Its use with N-trifluoracetyl (TFA)-protected isoleucine and allo-isoleucine is described. The 1H-NMR of the α-proton signal offers a convenient way to monitor the chirality retention in the acid chloride forming reaction and subsequent Friedel-Crafts acylation of arenes which result in α-amino acid aryl-ketone with no loss of chirality.


1991 ◽  
Vol 56 (8) ◽  
pp. 2635-2642 ◽  
Author(s):  
Louis A. Carpino ◽  
Hann Guang Chao ◽  
Michael Beyermann ◽  
Michael Bienert

ChemInform ◽  
2010 ◽  
Vol 30 (13) ◽  
pp. no-no
Author(s):  
Hosahudya N. Gopi ◽  
Vommina V. Suresh Babu
Keyword(s):  

Peptides ◽  
1988 ◽  
pp. 189-191 ◽  
Author(s):  
Michael Beyermann ◽  
Dörthe Granitza ◽  
Michael Bienert ◽  
Burghard Mehlis ◽  
Hartmut Niedrich ◽  
...  

Peptides ◽  
1992 ◽  
pp. 564-565
Author(s):  
D. S. Perlow ◽  
P. D. Williams ◽  
R. D. Tung ◽  
R. M. Freidinger ◽  
F. M. F. Chen ◽  
...  

1989 ◽  
Vol 54 (6) ◽  
pp. 1746-1752 ◽  
Author(s):  
Jutta Eichler ◽  
Michael Beyermann ◽  
Michael Bienert

Cellulose paper was esterified with Nα-Fmoc-protected amino acid chlorides providing a chemically stable segmental support, the utility of which for simultaneous solid phase peptide synthesis was demonstrated by the synthesis of several sets of model peptides following different synthetic strategies.


ChemInform ◽  
2010 ◽  
Vol 22 (39) ◽  
pp. no-no
Author(s):  
L. A. CARPINO ◽  
H. G. CAHO ◽  
M. BEYERMANN ◽  
M. BIENERT

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