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Nickel-Catalyzed anti-Selective Alkyne Functionalization Reactions
Synthesis ( IF 2.2 ) Pub Date : 2020-06-22 , DOI: 10.1055/s-0040-1707885
Dale J. Wilger 1 , Sydney E. Bottcher , Lauren E. Hutchinson
Affiliation  


Abstract

Nickel-catalyzed anti-selective alkyne functionalization reactions are reviewed with an emphasis on the mechanisms that lead to their observed stereoselectivity. Since the isomerization of alkenylnickel species plays a key role in a large number of these reactions, the potential mechanisms for these processes are also described in detail.

1 Introduction

2 anti-Selective Hydroarylation

3 anti-Selective Carboborylation

4 anti-Selective Dicarbofunctionalization

4.1 Carbocyanative Cyclization

4.2 Cyclization with Aryl Donors

4.3 Cyclization with CO2

4.4 Intermolecular Dicarbofunctionalization

5 anti-Selective Carbosulfonylation

6 Alkenylnickel Isomerization

7 Conclusions



中文翻译:

镍催化的抗选择性炔烃官能化反应


摘要

综述了镍催化的选择性炔烃官能化反应,重点是导致其立体选择性的机理。由于烯基镍物种的异构化在许多此类反应中起着关键作用,因此,还将详细描述这些过程的潜在机理。

1引言

2选择性氢芳基化

3选择性碳硼化

4选择性二碳官能化

4.1碳氰化环化

4.2与芳基供体的环化

4.3用CO 2环化

4.4分子间双碳官能化

5选择性磺酰化

6烯基镍异构化

7结论

更新日期:2020-06-23
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