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The Diversity and Evolution of Chiral Brønsted Acid Structures
被引:2
作者:
Handjaya, Jasemine P.
[1
]
Patankar, Niraja
[1
]
Reid, Jolene P.
[1
]
机构:
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
Br & oslash;
nsted Acid;
Catalyst Design;
Enantioselectivity;
Reaction Mechanism;
Noncovalent Interactions;
CATALYTIC ASYMMETRIC-SYNTHESIS;
FRIEDEL-CRAFTS REACTION;
DIELS-ALDER REACTION;
BRONSTED-ACID;
ENANTIOSELECTIVE SYNTHESIS;
TRANSFER HYDROGENATION;
BOND DONORS;
METAL-FREE;
DESYMMETRIZATION;
ACTIVATION;
D O I:
10.1002/chem.202400921
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The chemical space of chiral Br & oslash;nsted acid catalysts is defined by quantity and complexity, reflecting the diverse synthetic challenges confronted and the innovative molecular designs introduced. Here, we detail how this successful outcome is a powerful demonstration of the benefits of utilizing both local structure searches and a comprehensive understanding of catalyst performance for effective and efficient exploration of Br & oslash;nsted acid properties. In this concept article we provide an evolutionary overview of this field by summarizing the approaches to catalyst optimization, the resulting structures, and functions. The number and complexity of chiral Br & oslash;nsted acids are dramatically increasing, ultimately leading to unique generations of catalysts with enhanced reaction capabilities. In this concept article, we discuss how the approach to optimizing these structures have transitioned from foundational structural tuning to a function-driven approach. image
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