-transparent.png){kind=logo}
Catalytic enantioselective [2 + 2] cycloadditions between allenoates and alkenes is disclosed. The method functions well for a variety of alkenes, and the products are generated with excellent levels of enantioselectivity. One of the most significant aspects of the present method is that unactivated alkenes are suitable substrates for this method, which is distinctly different from nearly all other catalytic enantioselective [2 + 2] cycloaddition methods.
| UI | MeSH Term | Description | Entries |
|---|
Related Publications
Michael L Conner, and
Yao Xu, and
M Kevin Brown
April 2004,
Proceedings of the National Academy of Sciences of the United States of America,
Michael L Conner, and
Yao Xu, and
M Kevin Brown
October 2018,
Angewandte Chemie (International ed. in English),
Michael L Conner, and
Yao Xu, and
M Kevin Brown
June 2019,
Tetrahedron,
Michael L Conner, and
Yao Xu, and
M Kevin Brown
November 2009,
Organic letters,
Michael L Conner, and
Yao Xu, and
M Kevin Brown
October 2002,
Chemical communications (Cambridge, England),
Michael L Conner, and
Yao Xu, and
M Kevin Brown
September 2016,
The Journal of organic chemistry,
Michael L Conner, and
Yao Xu, and
M Kevin Brown
December 2023,
Angewandte Chemie (International ed. in English),
Michael L Conner, and
Yao Xu, and
M Kevin Brown
September 2021,
Angewandte Chemie (International ed. in English),
Michael L Conner, and
Yao Xu, and
M Kevin Brown
February 2013,
Journal of the American Chemical Society,
Michael L Conner, and
Yao Xu, and
M Kevin Brown
January 2003,
The Journal of organic chemistry,
