| dc.contributor.author |
Bajaj, Kiran |
|
| dc.date.accessioned |
2021-11-11T11:23:28Z |
|
| dc.date.available |
2021-11-11T11:23:28Z |
|
| dc.date.issued |
2012-09-14 |
|
| dc.identifier.uri |
https://onlinelibrary.wiley.com/doi/10.1111/cbdd.12053 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3503 |
|
| dc.description.abstract |
Unprotected S-acylated cysteine isopeptides containing α-, β- or γ-amino acid units have been synthesized, and their conversion to native hexapeptides by S- to the N-terminus ligations involving 17-, 18- and 19-membered cyclic transition states have been demonstrated both experimentally and computationally to be more favorable than intermolecular cross-ligations. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Chemical Ligation |
en_US |
| dc.subject |
19-Membered Cyclic |
en_US |
| dc.title |
Study of Chemical Ligation Via 17-, 18- and 19-Membered Cyclic Transition States |
en_US |
| dc.type |
Article |
en_US |