Synthesis of 2′ protected nucleosides
AssigneeHongene Biotech Corporation
InventorsWing C. Poon, Ruiming Zou, Aldrich N. K. Lau, David Yu, Gengyu Du, Yun-Chiao Yao, Gang Zhao
Life of this patent
Estimating the term…
Loading patent…
AssigneeHongene Biotech Corporation
InventorsWing C. Poon, Ruiming Zou, Aldrich N. K. Lau, David Yu, Gengyu Du, Yun-Chiao Yao, Gang Zhao
Estimating the term…
Embodiments of the present application relate to the preparation of 2′-O-protected nucleoside phosphoramidites and conjugation of the 2′-O-protected nucleoside to a solid support. More specifically, the present application relates to nucleosides having a hydroxy protecting group at the 2′ position that reduces migration to the 3′ position during RNA (e.g., mRNA) synthesis and can be readily removed under mild conditions without the use of toxic metal-containing reagents. Methods of using the nucleosides described herein in RNA synthesis are also disclosed.
A compound of Formula (I):
A method of deprotecting an oligonucleotide or polynucleotide comprising at least one 2′ protected nucleotide residue comprising the structure of Formula (II):
A solid support bound oligonucleotide or polynucleotide comprising at least one 2′ protected nucleotide residue comprising the structure of Formula (II):
Dependencies are inferred from the claim text.