Fast and efficient chemical ligation of oligonucleotides using diels-alder reaction.
Diels-Alder chemical ligation was applied to the ligation of two and three oligonucleotides to form a single, continuous strand with an unnatural DNA backbone at the ligation site. The reaction occurred between a maleimide-labelled oligonucleotide and a furan-labelled oligonucleotide to form two ty...
Saved in:
Main Author: | Cheong, Vee Vee. |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Final Year Project |
Language: | English |
Published: |
2010
|
Subjects: | |
Online Access: | http://hdl.handle.net/10356/39857 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
A modular approach to enzymatic ligation of peptides and proteins with oligonucleotides
by: Tan, Derrick Jing Yang, et al.
Published: (2022) -
Enantioselective Diels–Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes
by: Fang, Xinqiang, et al.
Published: (2014) -
Formal Diels-Alder reactions of chalcones and formylcyclopropanes catalyzed by chiral N-heterocyclic carbenes
by: Lv, Hui, et al.
Published: (2014) -
Asymmetric synthesis of functionalized chiral diphosphines via organopalladium promoted hydrophosphination and diels-alder reactions
by: Yuan, Mingjun
Published: (2011) -
Asymmetric Diels-Alder reactions of N-allenoyloxazolidinones catalyzed by Cu(II)-bis(oxazoline) complexes
by: Torsak Luanphaisarnnont
Published: (2018)