## Abstract The synthesis is described of the protected linear decapeptide: __N__‐benzyloxycarbonyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐tyrosyl‐__L__‐tyrosyl‐__L__‐phenylalanyl‐__L__‐glutaminyl‐__L__‐asparaginyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐prolyl‐__N__^6^‐tosyl‐__L__‐lysylglycineamide (II, Fi
Synthesis of a tyrosine “homologue” of lysine-vasotocin
✍ Scribed by H. C. Beyerman; J. S. Bontekoe
- Book ID
- 104586235
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 264 KB
- Volume
- 79
- Category
- Article
- ISSN
- 0165-0513
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis is described of the protected linear decapeptide: N‐benzyloxycarbonyl‐S‐benzyl‐L‐cysteinyl‐L‐tyrosyl‐L‐tyrosyl‐L‐isoleucyl‐L‐glutaminyl‐L‐asparaginyl‐S‐benzyl‐L‐cysteinyl‐L‐prolyl‐N^e^‐tosyl‐L‐lysylglycineamide (II, Fig. 2).
Removal of the blocking groups from II, followed by oxidation, yielded a preparation assumed to contain a “homologue” of lysine‐vasotocin with two consecutive molecules of tyrosine instead of one (Fig. 1, n = 2).
📜 SIMILAR VOLUMES
## Abstract A synthesis is described of the “protected” decapeptide __N__‐benzyloxycarbonyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐tyrosyl‐__L__‐tyrosyl‐__L__‐isoleucyl‐__L__‐glutaminyl‐__L__‐asparaginyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐prolyl‐__L__‐leucylglycineamide (V). Removal of the blocking gr
## Abstract The synthesis is described of the protected linear decapeptide: __N__‐benzyloxycarbonyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐tyrosyl‐__L__‐tyrosyl‐__L__‐phenylalanyl‐__L__‐glutaminyl‐__L__‐asparaginyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐prolyl‐__L__‐leucylglycineamide (III, Fig. 2). Remov
## Abstract The synthesis is described of the protected linear nonapeptide: __N__‐benzyloxycarbonyl‐__S__‐benzyl‐L‐cysteinyl‐__L__‐tyrosyl‐__L__‐tyrosyl‐__L__‐glutammyl‐__L__‐asparaginyl‐__S__‐benzyl‐__L__‐cysteinyl‐__L__‐prolyl‐__N__^e^‐__p__‐toluenesulfonyl‐__L__‐lysylglycineamide (II, Fig. 2) in
## Abstract Sequential polypeptides with the repeating units L‐tyrosyl‐L‐lysyl, L‐tyrosyl‐(L‐lysyl)~2~, and L‐tyrosyl‐(L‐lysyl)~3~ have been synthesized by solution polymerization of the __N__‐hydroxy‐succinimide esters of the corresponding di‐, tri‐, and tetrapeptides. The monomers for the polytri