Enantioselective Construction of Spiro[2H-pyran-3,4′-indoline] by a Systematic Michael/Reduction/Cyclization Sequence Triggered by the Asymmetric Conjugate Addition of Ketones to Isatylidenemalononitriles-Reference-Cited by-同舟云学术

Enantioselective Construction of Spiro[2H-pyran-3,4′-indoline] by a Systematic Michael/Reduction/Cyclization Sequence Triggered by the Asymmetric Conjugate Addition of Ketones to Isatylidenemalononitriles

Published:2012-02-21 Issue:10 Volume:2012 Page:1935-1944
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Zhao Hua,Lan Yu-Bao,Liu Zhao-Min,Wang Yong,Wang Xing-Wang,Tao Jing-Chao

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference110 articles.

1. Preparation of 3-spirocyclic indolin-2-ones as ligands for the ORL-1 receptor

2. Absolute Stereochemistry of Citrinadins A and B from Marine-Derived Fungus

3. Design, Synthesis, and SAR of New Pyrrole-Oxindole Progesterone Receptor Modulators Leading to 5-(7-Fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile (WAY-255348)

4. Isolation, Structure Elucidation, and Biomimetic Total Synthesis of Versicolamide B, and the Isolation of Antipodal (−)-Stephacidin A and (+)-Notoamide B fromAspergillus versicolor NRRL 35600

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