Journal
ACS CATALYSIS
Volume 12, Issue 17, Pages 10603-10620Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c02857
Keywords
boron; vicinal boronates; Suzuki-Miyaura cross-coupling; 1,2-shift; boronate allylation; site-selective functionalization; boro-Wittig reaction
Categories
Funding
- MICINN [PID2019- 107380GB-I00]
Ask authors/readers for more resources
Selective functionalization of the C-B bond in 1,2-bis(boronate) esters allows for the preparation of 1,2-difunctionalized compounds with stereocontrol, making them useful in the synthesis of complex molecules.
Selective functionalization of the C-B bond in 1,2-bis(boronate) esters has emerged as a powerful tool to prepare 1,2-difunctionalized compounds with stereocontrol. Selective Suzuki cross-coupling, oxidation, amination, and homologation reactions serve as platforms to prepare a wide variety of compounds from a common intermediate. The exquisite selectivity offered and their easy preparation from feedstock material using a myriad of catalytic transformations make them attractive building blocks for the preparation of complex molecules. In this Perspective, we summarize the examples of selective C-B bond functionalization of vicinal bis(boronates), attending to the nature of the C-B bond functionalization.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available