Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species-Reference-Cited by-同舟云学术

Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species

Published:2018-04-04 Issue:8 Volume:83 Page:4568-4580
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fujita Hikaru¹^ORCID,Kakuyama Satoshi¹,Fukuyoshi Shuichi¹,Hayakawa Naoko¹,Oda Akifumi²,Kunishima Munetaka¹^ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan

2. Graduate School of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya, Aichi 468-8503, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00331

Reference61 articles.

1. Stereocontrolled Glycosyl Transfer Reactions with Unprotected Glycosyl Donors

2. Recent advances in heterolytic nucleofugal leaving groups

3. Contemporary Carbocation Chemistry: Applications in Organic Synthesis

4. Electrostatic Activation of Nucleofuges: Cationic Leaving Groups

5. Fluorodesulfurization. A new reaction for the formation of carbon-fluorine bonds

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