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Dylan Moran

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Articles

Cyclic sulfone ring remodeling enables molecular shape diversity-oriented synthesis of privileged biaryl and oligoaryl motifs

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By Viet D. Nguyen, Sachchida Nand, Ramón Treviño Verified, Arka Porey, William Thompson, Graham C. Haug, Seth O. Fremin, Shree Krishna Dhakal, William Hughes, Dylan Moran, Johant Lakey-Beitia, Chandan Giri, Samuel G. Greco, Hadi Arman, Oleg V. Larionov, Patrick Manning-Lorino
| Nature Verified
Abstract Molecular shape is a key determinant of the structural properties and intermolecular interactions of privileged scaffolds, such as biaryl and oligoaryl compounds, which are widely used in the design of drugs, catalysts, and functional materials. Despite the well-recognized importance of molecular shape diversity and increased three-dimensionality, the chemical space of biaryl compounds remains dominated by linear and disk-like structures featuring para and meta substitution patterns.
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Catalytic Asymmetric Total Synthesis of Grisemycin, a Thioangucycline Polyketide Click to copy article link Article link copied!

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By Kincade Stevenson, Dylan Moran, Thomas J. Maimone
| ACS Publications
Cite Jump to ExpandCollapse CommunicationMarch 13, 2026 Catalytic Asymmetric Total Synthesis of Grisemycin, a Thioangucycline Polyketide Click to copy article linkArticle link copied! Kincade Stevenson Kincade Stevenson Department of Chemistry, University of California-Berkeley, 826 Latimer Hall, Berkeley, California 94720, United States Dylan P. Moran Dylan P. Moran Department of Chemistry, University of California-Berkeley, 826 Latimer Hall, Berkeley, California 94720, United States Thomas J.
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Catalytic Asymmetric Total Synthesis of Grisemycin, a Thioangucycline Polyketide Click to copy article link Article link copied!

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By Kincade Stevenson, Dylan Moran, Thomas J. Maimone
| dx.doi.org
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