高等学校化学学报 ›› 2020, Vol. 41 ›› Issue (7): 1426.doi: 10.7503/cjcu20200090
• 庆祝《高等学校化学学报》复刊40周年专栏 • 上一篇 下一篇
收稿日期:
2020-02-20
出版日期:
2020-07-10
发布日期:
2020-04-08
通讯作者:
朱守非
E-mail:sfzhu@nankai.edu.cn
基金资助:
Received:
2020-02-20
Online:
2020-07-10
Published:
2020-04-08
Contact:
Shoufei ZHU
E-mail:sfzhu@nankai.edu.cn
Supported by:
摘要:
从不对称催化的角度总结了近年来碳硼成键反应的研究进展, 评述了这些反应各自的特点, 并对其未来研究进行了展望.
中图分类号:
TrendMD:
黄明耀, 朱守非. 催化不对称碳硼成键反应研究进展. 高等学校化学学报, 2020, 41(7): 1426.
HUANG Mingyao, ZHU Shoufei. Recent Advances of Catalytic Asymmetric C—B Bond Forming Reactions†. Chem. J. Chinese Universities, 2020, 41(7): 1426.
Scheme 4 Cu-catalyzed asymmetric protoboration of alkeneswith different ligands (A) Bisphosphorous ligand L2; (B) bisphosphorous ligand L1; (C) diamine ligands; (D) NHC ligands; (E) bipyridine ligands.
Scheme 5 Cu(Ⅱ)/L5-catalyzed asymmetric 1,6-protoboration of α,β,γ,δ-unsaturated compounds(A) and Cu(Ⅰ)/L1-catalyzed asymmetric 1,6-protoboration of α,β,γ,δ-unsaturated compounds(B)
Scheme 9 Cu(Ⅰ)/L10-catalyzed asymmetric protoboration of imines(A), Cu(Ⅰ)/L11-catalyzed asymmetric protoboration of imines(B) and Cu/L12-catalyzed asymmetric protoboration of aldehydes(C)
Scheme 12 Rh(Ⅰ)-catalyzed asymmetric diboration of 1,2-disubstituted alkenes(A), Pd(0)-catalyzed asymmetric diboration of allenes(B), Pt(0)-catalyzed 1,4-diboration of conjugated dienes(C) and Pt(0)-catalyzed 1,2-diboration of conjugated dienes(D)
Scheme 14 Alcohol-catalyzed asymmetric diboration of alkenes (A) C4-catalyzed diboration; (B) C5-catalyzed diboration; (C) proposed mechanismof C4-catalyzed diboration; (D) proposed mechanismof C5-catalyzed diboration.
Scheme 18 Cu-catalyzed asymmetric carboration of allenes with aldehydes and ketones(A) and Cu-catalyzed asymmetric carboration of allenes with imines(B)
Scheme 19 Pd(Ⅱ)/L23-catalyzed asymmetric arylboration of alkenes(A), Pd(Ⅱ)/L24-catalyzed asymmetric arylboration of alkenes(B) and proposed mechanism(C)
Scheme 23 Ir(Ⅲ)-catalyzed asymmetric C(sp2)—H borylation of diarylmethylamines(A) and Ir(Ⅲ)-catalyzed kinetic resolution through C(sp2)—H borylation of diarylmethylamines(B)
Scheme 24 Cu(Ⅰ)-catalyzed asymmetric borylation of allylic carbonates(A), Cu(Ⅰ)-catalyzed asymmetric borylation of (γ-alkoxyallyl)boronates(B) and proposed mechanism(C)
Scheme 25 Cu(Ⅰ)-catalyzed enantioselective borylation of allylic carbonates(A) and Cu(Ⅰ)-catalyzed asymmetric stereo-convergent borylation of allylic carbonates(B)
Scheme 30 Rh(Ⅲ)-catalyzed asymmetric B—H bond insertion reaction of diazoketones and diazoesters(A), Cu(Ⅰ)-catalyzed asymmetric B—H bond insertion reaction of α-trifluo methyl diazocompounds(B) and genetically programmed synthesis of chiral organoboranes(C)
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