Deprotection of N-Alloc amines by Pd(0)/DABCO—an efficient method for in situ peptide coupling of labile amino acids

2001 ◽  
Vol 42 (40) ◽  
pp. 7049-7053 ◽  
Author(s):  
Chiara Zorn ◽  
Frieder Gnad ◽  
Sunnhild Salmen ◽  
Timothy Herpin ◽  
Oliver Reiser
Keyword(s):  
Amino Acids ◽  
Efficient Method ◽  
Peptide Coupling

ChemInform Abstract: Deprotection of N-Alloc Amines by Pd(0)/DABCO - An Efficient Method for in situ Peptide Coupling of Labile Amino Acids.

ChemInform ◽  
2010 ◽  
Vol 33 (2) ◽  
pp. no-no
Author(s):  
Chiara Zorn ◽  
Frieder Gnad ◽  
Sunnhild Salmen ◽  
Timothy Herpin ◽  
Oliver Reiser
Keyword(s):  
Amino Acids ◽  
Efficient Method ◽  
Peptide Coupling

A facile one pot route for the synthesis of imide tethered peptidomimetics

2016 ◽  
Vol 14 (2) ◽  
pp. 556-563 ◽  
Author(s):  
Veladi Panduranga ◽  
Girish Prabhu ◽  
Roopesh Kumar ◽  
Basavaprabhu Basavaprabhu ◽  
Vommina V. Sureshbabu
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Efficient Method ◽  
One Pot ◽  
Protected Amino Acid

A simple and efficient method for the synthesis of N,N’-orthogonally protected imide tethered peptidomimetics is presented. The imide peptidomimetics were synthesized by coupling the in situ generated selenocarboxylate of Nα-protected amino acids with Nα-protected amino acid azides in good yields.

Peptide Coupling of Unprotected Amino Acids Through in situ p-Nitrophenyl Ester Formation.

ChemInform ◽  
2003 ◽  
Vol 34 (2) ◽  
Author(s):  
Paul Gagnon ◽  
Xicai Huang ◽  
Eric Therrien ◽  
Jeffrey W. Keillor
Keyword(s):  
Amino Acids ◽  
Peptide Coupling ◽  
Ester Formation ◽  
Nitrophenyl Ester

Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation

2002 ◽  
Vol 43 (43) ◽  
pp. 7717-7719 ◽  
Author(s):  
Paul Gagnon ◽  
Xicai Huang ◽  
Eric Therrien ◽  
Jeffrey W. Keillor
Keyword(s):  
Amino Acids ◽  
Peptide Coupling ◽  
Ester Formation ◽  
Nitrophenyl Ester

scholarly journals An Efficient Method for the Reduction of N-Protected Amino Acids and Peptides to the Corresponding Alcohols

1999 ◽  
Vol 23 (7) ◽  
pp. 424-425
Author(s):  
T. Naqvi ◽  
M. Bhattacharya ◽  
W. Haq
Keyword(s):  
Amino Acids ◽  
Efficient Method

Reduction of pentachlorophenyl esters of Boc protected amino acids and peptides to the corresponding alcohols is described.

In situ studies on alginic acid synthesis and other aspects of the metabolism of Laminaria digitata

1972 ◽  
Vol 50 (1) ◽  
pp. 177-184 ◽  
Author(s):  
Johan A. Hellebust ◽  
Arne Haug
Keyword(s):  
Amino Acids ◽  
Time Course ◽  
Alginic Acid ◽  
Acid Synthesis ◽  
Short Term ◽  
Fresh Weight Basis ◽  
Mannuronic Acid ◽  
Guluronic Acid ◽  
Rate Of Photosynthesis

Amino acids, particularly alanine and aspartate, become more strongly labeled than mannitol in short-term 14C-photoassimilation experiments. The amino acids are the most likely sources of carbon for alginic acid synthesis and respiration in the dark, in contrast to mannitol, which appears to be relatively unavailable. Temperature is very important in determining the rate of loss of recent photoassimilate in L. digitata. The rate of photosynthesis, on a fresh weight basis, is much higher for blades than for stipes.The time course for incorporation of photoassimilated carbon into alginate differs for the stipe and blade both in light and dark periods. Very little 14C enters alginate in blades in the dark, while alginate in stipes acquires considerable amounts of activity during dark periods. Alginate in both blade and stipe acquires 14C predominantly in mannuronic acid residues of their alginate during short-term photoassimilation periods, while guluronic acid residues become relatively more rapidly labeled during dark periods.

scholarly journals Innentitelbild: In Situ Probing of Newly Synthesized Peptidoglycan in Live Bacteria with FluorescentD-Amino Acids (Angew. Chem. 50/2012)

2012 ◽  
Vol 124 (50) ◽  
pp. 12546-12546
Author(s):  
Erkin Kuru ◽  
H. Velocity Hughes ◽  
Pamela J. Brown ◽  
Edward Hall ◽  
Srinivas Tekkam ◽  
...  
Keyword(s):  
Amino Acids ◽  
Live Bacteria
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