Tributylphosphane-promoted (3 +2) annulation of 3-hydroxyoxindoles with acrylates : synthesis of spirocyclic oxindole-lactones
Joint Authors
Jin, Qiaomei
Hu, Shihe
Zhang, Jian
Source
Journal of Saudi Chemical Society
Issue
Vol. 22, Issue 1 (31 Jan. 2018), pp.27-33, 7 p.
Publisher
Publication Date
2018-01-31
Country of Publication
Saudi Arabia
No. of Pages
7
Main Subjects
Abstract EN
The tributylphosphane-promoted [3 +2] annulation reactions of 3-hydroxyoxindoles with acrylates have been developed to give a variety of pharmaceutically attractive spirocyclic oxindole-lactone derivatives in good to excellent yields.
The structures of all the compounds were confirmed by 1H NMR, 13C NMR and HRMS.
This metal-free procedure features low costs of the reagents and materials, mild reaction conditions, non-toxicity and easy handling for scalable synthesis.
American Psychological Association (APA)
Jin, Qiaomei& Zhang, Jian& Hu, Shihe. 2018. Tributylphosphane-promoted (3 +2) annulation of 3-hydroxyoxindoles with acrylates : synthesis of spirocyclic oxindole-lactones. Journal of Saudi Chemical Society،Vol. 22, no. 1, pp.27-33.
https://search.emarefa.net/detail/BIM-787934
Modern Language Association (MLA)
Jin, Qiaomei…[et al.]. Tributylphosphane-promoted (3 +2) annulation of 3-hydroxyoxindoles with acrylates : synthesis of spirocyclic oxindole-lactones. Journal of Saudi Chemical Society Vol. 22, no. 1 (Jan. 2018), pp.27-33.
https://search.emarefa.net/detail/BIM-787934
American Medical Association (AMA)
Jin, Qiaomei& Zhang, Jian& Hu, Shihe. Tributylphosphane-promoted (3 +2) annulation of 3-hydroxyoxindoles with acrylates : synthesis of spirocyclic oxindole-lactones. Journal of Saudi Chemical Society. 2018. Vol. 22, no. 1, pp.27-33.
https://search.emarefa.net/detail/BIM-787934
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 33
Record ID
BIM-787934