Kinetic Study on Michael-Type Reactions of β-Nitrostyrenes with Cyclic Secondary Amines in Acetonitrile: Transition-State Structures and Reaction Mechanism Deduced from Negative Enthalpy of Activation and Analyses of LFERs-Reference-Cited by-同舟云学术

Kinetic Study on Michael-Type Reactions of β-Nitrostyrenes with Cyclic Secondary Amines in Acetonitrile: Transition-State Structures and Reaction Mechanism Deduced from Negative Enthalpy of Activation and Analyses of LFERs

Published:2013-05-17 Issue:11 Volume:78 Page:5604-5610
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Um Ik-Hwan¹,Kang Ji-Sun¹,Park Jong-Yoon¹

Affiliation:

1. Department of Chemistry and Division of Nano Sciences and ‡Department of Science Education, Ewha Womans University, Seoul 120-750, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo4007442

Reference71 articles.

1. aSmith, M. B. and March, J.March’s Advanced Organic Chemistry,5th ed.Wiley-Interscience:New York, 2001; p976.

2. bLowry, T. H. and Richardson, K. S.Mechanism and Theory in Organic Chemistry,3rd ed.Harper Collins Publishers:New York, 1987; p622.

3. cCarey, F. A. and Sundberg, R. J.Advanced Organic Chemistry Part B: Reactions and Synthesis,3rd ed.Plenum Press:New York, 1990; pp39–46.

4. A Redox-Reconfigurable, Ambidextrous Asymmetric Catalyst

5. Refined Transition-State Models for Proline-Catalyzed Asymmetric Michael Reactions under Basic and Base-Free Conditions

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