Origins of Diastereoselectivity of 1,3-Dipolar Cycloadditions of Cyclic Azomethine Ylides and Nitrones to Cyclopentenes
-selective pathways. These contrasting reactivity and selectivity trends result from the different electronic and steric effects of the two 1,3-dipoles.
Authors
- Pengchen Ma (ORCID: https://orcid.org/0000-0002-4110-4696)
- X D Liu
- Silong Xu (ORCID: https://orcid.org/0000-0003-3279-9331)
- Shuangshuang Cai
- K N Houk
- Shaohong Wang
- Xin-Hua Duan (ORCID: https://orcid.org/0000-0002-1527-5934)
Institutions
- Xi'an University of Science and Technology (CN)
- Battery Park (US)
- University of California System (US)
- Hubei University of Automotive Technology (CN)
- Xi'an Jiaotong University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-05-10
- DOI
- https://doi.org/10.1021/acs.joc.6c00133
- Primary Topic
- Organic Chemistry Cycloaddition Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00