Enantioselective Construction of Eight‐Membered N‐Heterocycles from Simple 1,3‐Dienes via Pd(0) Lewis Base Catalysis

Author:

Pan Jiaoting12,Ho Takumi Ogawa2,Chen Ying‐Chun3,Yang Bin‐Miao1,Zhao Yu12ORCID

Affiliation:

1. Joint School of National University of Singapore and Tianjin University International Campus of Tianjin University Binhai New City Fuzhou 350207 China

2. Department of Chemistry National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore

3. Key Laboratory of Drug-Targeting and Drug Delivery System of the Ministry of Education and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy Sichuan University Chengdu 610041 P. R. China

Abstract

AbstractWe report herein an unprecedented enantioselective (4+4) cycloaddition of simple 1,3‐dienes with azadienes for the construction of fused eight‐membered N‐heterocycles. In this transformation, the π‐Lewis basic Pd(0) catalyst achieves activation of 1,3‐dienes to induce nucleophilic addition to azadienes followed by ring cyclization via a selective terminal allylic substitution. Furthermore, highly efficient and diastereoselective derivatizations of the eight‐membered rings provide a facile access to diverse enantiopure fused tetra‐ to hexacyclic compounds with potential application in medicinal chemistry.

Funder

Ministry of Education - Singapore

National Natural Science Foundation of China

National University of Singapore

Publisher

Wiley

Subject

General Medicine

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