Computational Studies on Reaction Mechanism and Origins of Selectivities in Nickel-Catalyzed (2 + 2 + 2) Cycloadditions and Alkenylative Cyclizations of 1,6-Ene–Allenes and Alkenes-Reference-Cited by-同舟云学术

Computational Studies on Reaction Mechanism and Origins of Selectivities in Nickel-Catalyzed (2 + 2 + 2) Cycloadditions and Alkenylative Cyclizations of 1,6-Ene–Allenes and Alkenes

Published:2017-01-31 Issue:4 Volume:82 Page:2150-2159
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yang Tao¹²^ORCID,Ehara Masahiro¹²

Affiliation:

1. Institute for Molecular Science and Research Center for Computational Science, Nishigonaka 38, Myodaiji, Okazaki 444-8585, Japan

2. Elements Strategy Initiative for Catalysts and Batteries (ESICB), Kyoto University, Kyoto 615-8520, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02957

Reference77 articles.

1. Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

2. Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis

3. Recent Advances in the Transition-Metal-Catalyzed Regioselective Approaches to Polysubstituted Benzene Derivatives

4. Allenes, versatile unsaturated motifs in transition-metal-catalysed [2+2+2] cycloaddition reactions

5. Alkenes in [2+2+2] Cycloadditions

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