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[3 + 2] cycloaddition of nonstabilized azomethine ylides and 2-benzothiazolamines to access imidazolidine derivatives.
Wang, Kai-Kai; Li, Yan-Li; Wang, Ming-Yue; Jing, Jun; Wang, Zhan-Yong; Chen, Rongxiang.
Affiliation
  • Wang KK; School of Pharmacy, Xinxiang University Xinxiang 453000 P. R. China chenhlmei@163.com zhanyongw@126.com +86 373-3683138.
  • Li YL; Key Laboratory of Nano-carbon Modified Film Technology Engineering of Henan Province Xinxiang 453000 P. R. China.
  • Wang MY; Medical College, Xinxiang University Xinxiang 453000 P. R. China.
  • Jing J; School of Pharmacy, Xinxiang University Xinxiang 453000 P. R. China chenhlmei@163.com zhanyongw@126.com +86 373-3683138.
  • Wang ZY; School of Pharmacy, Xinxiang University Xinxiang 453000 P. R. China chenhlmei@163.com zhanyongw@126.com +86 373-3683138.
  • Chen R; School of Pharmacy, Xinxiang University Xinxiang 453000 P. R. China chenhlmei@163.com zhanyongw@126.com +86 373-3683138.
RSC Adv ; 12(44): 28295-28298, 2022 Oct 04.
Article in En | MEDLINE | ID: mdl-36320509
ABSTRACT
A simple and practical method for the construction of 1,3,5-trisubstituted imidazolidine derivatives via [3 + 2] cycloaddition reaction has been developed. This reaction could smoothly proceed between nonstabilized azomethine ylides generated in situ and 2-benzothiazolamines to deliver a wide scope of differently substituted imidazolidines in high yields (up to 98%). The structure of one example was confirmed by X-ray single-crystal structure analysis.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2022 Document type: Article