Tetraborylation of <i>p</i>-Benzynes Generated by the Masamune–Bergman Cyclization through Reaction Design Based on the Reaction Path Network-Reference-Cited by-同舟云学术

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Tetraborylation of p-Benzynes Generated by the Masamune–Bergman Cyclization through Reaction Design Based on the Reaction Path Network

Published:2024-06-20 Issue:7 Volume:4 Page:2578-2584
ISSN:2691-3704
Container-title:JACS Au
language:en
Short-container-title:JACS Au

Author:

Nakatsuka Soichiro¹²^ORCID,Akiyama Seiji¹³^ORCID,Harabuchi Yu¹³^ORCID,Maeda Satoshi¹²³⁴^ORCID,Nagata Yuuya¹³^ORCID

Affiliation:

1. ERATO Maeda Artificial Intelligence in Chemical Reaction Design and Discovery Project, JST, Sapporo 060-0810, Hokkaido, Japan

2. Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Hokkaido, Japan

3. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo 001-0021, Hokkaido, Japan

4. Research and Services Division of Materials Data and Integrated System (MaDIS), National Institute for Materials Science (NIMS), Tsukuba 305-0044, Ibaraki, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Exploratory Research for Advanced Technology

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacsau.4c00302

Reference44 articles.

1. Boronolectins and fluorescent boronolectins: An examination of the detailed chemistry issues important for the design

2. Boronic acids in medicinal chemistry: anticancer, antibacterial and antiviral applications

3. Boron Containing Compounds as Protease Inhibitors

4. Synthesis and Applications of Boronic Acid-Containing Polymers: From Materials to Medicine

5. Boron: Boranes in organic synthesis

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