1956
DOI: 10.1021/jo01110a017
|View full text |Cite
|
Sign up to set email alerts
|

The Use of Water-Soluble and Basic Carbodiimides in Peptide Synthesis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
50
0
4

Year Published

1978
1978
2013
2013

Publication Types

Select...
5
4
1

Relationship

0
10

Authors

Journals

citations
Cited by 216 publications
(54 citation statements)
references
References 0 publications
0
50
0
4
Order By: Relevance
“…We also successfully prepared water-dispersible Boc-Tyr(BrZ)-OH, which has a hydrophobic BrZ side chain protecting group [11]. WSCI [31], DMTMM [32,33] and combinations of an additive sulfo-HOSu [34] were examined [24]. Reaction temperature was 70 °C using a MW power of 70 W (Figure 1).…”
Section: Resultsmentioning
confidence: 99%
“…We also successfully prepared water-dispersible Boc-Tyr(BrZ)-OH, which has a hydrophobic BrZ side chain protecting group [11]. WSCI [31], DMTMM [32,33] and combinations of an additive sulfo-HOSu [34] were examined [24]. Reaction temperature was 70 °C using a MW power of 70 W (Figure 1).…”
Section: Resultsmentioning
confidence: 99%
“…The crosslinking agents used in collagen-rich biomaterials can use both primary amino groups and acid groups of polypeptide chains. Historically, a water soluble carbodiimide (1-ethyl-3-(3-dimethyl amino propyl) carbodiimide / EDAC) was first used for the modification of carboxylic groups in proteins for peptide synthesis (Sheehan & Hlavka, 1956) and to promote crosslinking in gelatin (Sheehan & Hlavka, 1957). The mechanism for the reaction between carboxylic groups and EDAC leading to amide bond formation is as follows: The addition of a carboxylic acid diimide produces an isourea ester, an O-acyl isourea.…”
Section: Tissue Crosslinking After Carboxylic Group Activationmentioning
confidence: 99%
“…The condensing agent used was I-cyclohexyl-3 (2-morpholinoethyl)-carbodiimide metho-p-toluene sulphonate (CMC). 4 Line et al? used CMC to immobilize pepsin onto amino-alkylated porous glass, and similarly Wondolowski and Woychick' immobilized p-galactosidase, although in both instances the activities of the resulting polymers were very low.…”
Section: Introductionmentioning
confidence: 99%