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

Saudi Chemical Society

Publication Date

2018-01-31

Country of Publication

Saudi Arabia

No. of Pages

7

Main Subjects

Chemistry

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