Citation: Junyan Chen, Dachang Bai, Xiuli Guo, Yiyao Wang, Xingwei Li. Diastereodivergent [4 + 2] annulation of biphenylenes with enones via nickel(0)-catalyzed C–C bond activation[J]. Chinese Chemical Letters, ;2022, 33(12): 5056-5060. doi: 10.1016/j.cclet.2022.02.079 shu

Diastereodivergent [4 + 2] annulation of biphenylenes with enones via nickel(0)-catalyzed C–C bond activation

Junyan Chen ^a ,
Dachang Bai ^{a, b, *,} ,
Xiuli Guo ^a ,
Yiyao Wang ^a ,
Xingwei Li ^{a, c, *,}

a.
NMPA Key Laboratory for Research and Evaluation of Innovative Drug, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China
b.
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
c.
School of Chemistry and Chemical Engineering, Shaanxi Normal University (SNNU), Xi'an 710062, China

baidachang@htu.edu.cn

lixw@snnu.edu.cn

Received Date: 12 November 2021
Revised Date: 25 February 2022
Accepted Date: 27 February 2022
Available Online: 4 March 2022

Figures(7)

Ni(0)-catalyzed regio- and diastereodivergent [4 + 2] annulation of biphenylenes with α, β unsaturated ketones is described. This solvent-controlled diastereodivergent reaction integrates C-C bond cleavage of biphenylene and C=C double bond insertion selectivity, offering a mild approach to all possible diastereoisomers of 9, 10-dihydrophenanthrene derivatives from the same starting materials.
- Nickel,
- Enones,
- Biphenylenes,
- Diastereodivergent annulation,
- C-C activation,
- 9, 10-Dihydrophenanthrenes
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