z-logo
Premium
3‐Chlorooxindoles: Versatile Starting Materials for Asymmetric Organocatalytic Synthesis of Spirooxindoles
Author(s) -
Noole Artur,
Ošeka Maksim,
Pehk Tõnis,
Öeren Mario,
Järving Ivar,
Elsegood Mark R. J.,
Malkov Andrei V.,
Lopp Margus,
Kanger Tõnis
Publication year - 2013
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201300019
Subject(s) - chemistry , organocatalysis , enantioselective synthesis , combinatorial chemistry , nanotechnology , organic chemistry , catalysis , materials science
3‐Chlorooxoindoles have emerged as versatile precursors in the synthesis of spirocyclopropyl oxindoles. High enantio‐ and diastereoselectivity was attained under conditions of both iminium/enamine and H‐bonding catalysis.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom