Highly E ‐Selective and Enantioselective Michael Addition to Electron‐Deficient Internal Alkynes Under Chiral Iminophosphorane Catalysis-Reference-Cited by-同舟云学术

Highly E ‐Selective and Enantioselective Michael Addition to Electron‐Deficient Internal Alkynes Under Chiral Iminophosphorane Catalysis

Published:2015-07 Issue:34 Volume:54 Page:9954-9957
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Uraguchi Daisuke¹,Yamada Kohei¹,Ooi Takashi¹²

Affiliation:

1. Institute of Transformative Bio‐Molecules (WPI‐ITbM) and Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Nagoya 464‐8603 (Japan)

2. CREST, Japan Science and Technology Agency (JST), Nagoya University, Nagoya 464‐8603 (Japan)

Funder

CREST-JST

Grant-in-Aid for Scientific Research

MEXT

JSPS

Asahi Glass Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201503928

Reference95 articles.

2. Alkynes in Organocatalysis

3. Organocatalytic transformations of alkynals, alkynones, propriolates, and related electron-deficient alkynes

4. For selected examples on the catalytic syntheses of β γ‐unsaturated carbonyl compounds see:

5. Organocatalytic Enantioselective Nucleophilic Vinylic Substitution

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