Enantioselective Organocatalytic Michael Addition and Ring Closure Cascade Reaction of o‐Quinone Methides with Nitriles

A convenient way to prepare chiral 2‐amino‐3‐substituted‐4H‐chromen derivatives.

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Bibliographic Details
Published inBulletin of the Korean Chemical Society Vol. 41; no. 5; pp. 570 - 573
Main Authors Park, Jin Wha, Jang, Subin, Choo, Mi Hyeon, Kim, Dae Young
Format Journal Article
LanguageEnglish
Published Weinheim Wiley‐VCH Verlag GmbH & Co. KGaA 01.05.2020
Wiley
대한화학회
Subjects
2‐amino‐4H‐chromene
Asymmetric catalysis
Chemistry
Chemistry, Multidisciplinary
Organocatalysis
o‐Quinone methides
Physical Sciences
Science & Technology
화학
o-Quinone methides
ASYMMETRIC CONJUGATE ADDITION
OXINDOLES
KETOACIDS
FLUORINATION
Asymmetric catalysis
Organocatalysis
BETA-KETO ACIDS
2-amino-4H-chromene
TETRAHYDROQUINOLINES
FRIEDEL-CRAFTS ALKYLATION
DECARBOXYLATIVE ALKYLATION
DERIVATIVES
NITROALKENES
Online AccessGet full text
ISSN1229-5949
0253-2964
1229-5949
DOI10.1002/bkcs.12011

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Summary:A convenient way to prepare chiral 2‐amino‐3‐substituted‐4H‐chromen derivatives.
Bibliography:https://onlinelibrary.wiley.com/doi/abs/10.1002/bkcs.12011
ISSN:1229-5949
0253-2964
1229-5949
DOI:10.1002/bkcs.12011