| Literature DB >> 28885017 |
Zachary L Niemeyer1, Suresh Pindi2, Dimitri A Khrakovsky2, Christian N Kuzniewski2, Cynthia M Hong2, Leo A Joyce3, Matthew S Sigman1, F Dean Toste2.
Abstract
Computed descriptors for acyclic diaminocarbene ligands are developed in the context of a gold catalyzed enantioselective tandem [3,3]-sigmatropic rearrangement-[2+2]-cyclization. Surrogate structures enable the rapid identification of parameters that reveal mechanistic characteristics. The observed selectivity trends are validated in a robust multivariate analysis facilitating the development of a highly enantioselective process.Entities:
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Year: 2017 PMID: 28885017 PMCID: PMC5903265 DOI: 10.1021/jacs.7b08791
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419