Synthesis of Asymmetrical-Terminally Bifunctionlized Alkanes by Sequential Suzuki-Miyaura Coupling Using B -Thexylboracyclanes
Author:
Affiliation:
1. Department of Applied Chemistry; Graduate School of Science and Engineering; Tokyo Institute of Technology; 2-12-1-H101 Ookayama 152-8552 Meguro Tokyo
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference36 articles.
1. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
2. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
3. Selection of boron reagents for Suzuki–Miyaura coupling
4. Palladium-catalyzed cross-coupling reactions of B-alkyl-9-BBN or trialkylboranes with aryl and 1-alkenyl halides
5. The B-Alkyl Suzuki-Miyaura Cross-Coupling Reaction: Development, Mechanistic Study, and Applications in Natural Product Synthesis
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2. Developments in the Synthesis of Mycobacterial Phenolic Glycolipids;The Chemical Record;2021-09-28
3. Synthesis of Lignans Based on a Borate‐mediated One‐pot Sequential Suzuki‐Miyaura Coupling of Cyclic Boranes;Chemistry – A European Journal;2021-05-19
4. A General Method for Photocatalytic Decarboxylative Hydroxylation of Carboxylic Acids;The Journal of Organic Chemistry;2020-03-05
5. Synthesis and Biological Evaluation of O‐Methylated Glycolipids Related to PGLs via Direct Stereoselective Glycosidation and Sequential Suzuki–Miyaura Coupling using Boracyclane;Chemistry – A European Journal;2017-10-24
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