3‐Isothiocyanato Oxindoles Serving as Powerful and Versatile Precursors to Structurally Diverse Dispirocyclic Thiopyrrolidineoxindoles through a Cascade Michael/Cyclization Process with Amino‐Thiocarbamate Catalysts | Zendy

Han WenYong | Zendy; Li ShiWu | Zendy; Wu ZhiJun | Zendy; Zhang XiaoMei | Zendy; Yuan WeiCheng | Zendy

Premium

3‐Isothiocyanato Oxindoles Serving as Powerful and Versatile Precursors to Structurally Diverse Dispirocyclic Thiopyrrolidineoxindoles through a Cascade Michael/Cyclization Process with Amino‐Thiocarbamate Catalysts

Author(s) -

Han WenYong,

Li ShiWu,

Wu ZhiJun,

Zhang XiaoMei,

Yuan WeiCheng

Publication year - 2013

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.201300206

Subject(s) - thiocarbamate , stereocenter , catalysis , computer science , combinatorial chemistry , process (computing) , chemistry , organic chemistry , enantioselective synthesis , operating system

Cascading catalysis : 3‐Isothiocyanato oxindoles act as powerful and versatile precursors for a range of structurally diverse dispirocyclic thiopyrrolidineoxindoles containing two spiro‐quaternary and three contiguous stereogenic centers in quantitative yields with excellent disatereo‐ and enantioselectivities by only using 1 mol % amino‐thiocarbamate catalyst.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research