Corrigendum to "One-pot tandem route to fused indolizidines and quinolizidines: Application in the synthesis of alkaloids and bioactive compounds" [Chinese Chemical Letters 32 (2021) 1713

Citation

Qiao Song, Yan Liu, Linlin Cai, Xinyu Cao, Shan Qian, Zhouyu Wang. Corrigendum to "One-pot tandem route to fused indolizidines and quinolizidines: Application in the synthesis of alkaloids and bioactive compounds" [Chinese Chemical Letters 32 (2021) 1713–1716][J]. Chin. Chem. Lett., 2022, 33(4): 2212-2212

Corrigendum to "One-pot tandem route to fused indolizidines and quinolizidines: Application in the synthesis of alkaloids and bioactive compounds" [Chinese Chemical Letters 32 (2021) 1713–1716]

Qiao Song^a, Yan Liu^b, Linlin Cai^b, Xinyu Cao^b, Shan Qian^a^,*, Zhouyu Wang^b^,*

^a Department of Pharmaceutics Engineering, Xihua University, Chengdu 610039, China;
^b Department of Chemistry, Xihua University, Chengdu 610039, China

Available online 24 January 2022

DOI of original article: 10.1016/j.cclet.2021.01.018
* Corresponding author.
E-mail addresses: qians33@163.com (S. Qian), zhouyuwang@mail.xhu.edu.cn (Z. Wang)

The authors regret that an interesting work about amide activation left uncited in the above-titled publication. An corrigendum is given as follows:

In 2017, Huang's group [1] reported an interesting method consisting of the amide activation (Tf₂O) induced dehydracoupling of halogenated secondary amides with alkenes and NaBH₄ reduction triggered tandem cyclization reaction. It is an efficient strategy to construct substituted pyrrolidine, piperidine, indolizidine, quinolizidine ring systems, and enimino carbocycles.


Chinese Chemical Letters 2022, Vol. 33 Issue (4): 2212-2212	PDF