cis-Tetrahydrofuran-3,4-diol Structure as a Key Skeleton of New Protecting Groups Removable by Self-Cyclization under Oxidative Conditions-Reference-Cited by-同舟云学术

cis-Tetrahydrofuran-3,4-diol Structure as a Key Skeleton of New Protecting Groups Removable by Self-Cyclization under Oxidative Conditions

Published:2006-08-26 Issue:20 Volume:71 Page:7668-7677
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Utagawa Eri¹,Sekine Mitsuo¹,Seio Kohji¹

Affiliation:

1. Department of Life Science, Tokyo Institute of Technology, 4259 Nagatsuta, Yokohama 226-8501, Japan, Frontier Collaborative Research Center, Tokyo Institute of Technology, 4259 Nagatsuta, Yokohama 226-8503, Japan, and CREST, Japan Science and Technology Agency, 4259 Nagatsuta, Yokohama 226-8501, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061006v

Reference38 articles.

1. Synthesis of pentathymidylate using a 4-monomethoxytritylthio (MMTrS) group as a 5′-hydroxyl protecting group: toward oligonucleotide synthesis without acid treatment

2. New Protected Protecting Groups for the 5′-Hydroxy Group of Deoxynucleosides by Use of 2-(Hydroxymethyl)- and 2-[(Methylamino)methyl]benzoyl Skeletons and Oxidatively Cleavable Tritylthio and (4-Methoxytrityl)thio Groups

3. A NEW PROTECTING GROUP FOR THE 5′-HYDROXYL GROUP HAVING O–S SINGLE BOND OXIDATIVELY CLEAVABLE UNDER MILD CONDITIONS

4. Solid-Phase Oligodeoxynucleotide Synthesis: A Two-Step Cycle Using Peroxy Anion Deprotection

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