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Julian A. Codelli

Researcher at California Institute of Technology

Publications -  12
Citations -  5003

Julian A. Codelli is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Enantioselective synthesis & Cycloaddition. The author has an hindex of 9, co-authored 12 publications receiving 4349 citations. Previous affiliations of Julian A. Codelli include University of California, Berkeley & University of California, Davis.

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Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders

TL;DR: A gut-microbiome-brain connection in a mouse model of ASD is supported and a potential probiotic therapy for GI and particular behavioral symptoms in human neurodevelopmental disorders is identified.
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Copper-free click chemistry for dynamic in vivo imaging

TL;DR: A Cu-free variant of click chemistry that can label biomolecules rapidly and selectively in living systems, overcoming the intrinsic toxicity of the canonical Cu-catalyzed reaction is reported.
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Second-Generation Difluorinated Cyclooctynes for Copper-Free Click Chemistry

TL;DR: A novel class of DIFO reagents for copper-free click chemistry that are considerably more synthetically tractable are reported and should expand the use of copper- free click chemistry in the hands of biologists.
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Fluorophore Targeting to Cellular Proteins via Enzyme-Mediated Azide Ligation and Strain-Promoted Cycloaddition

TL;DR: This work found that fluorophore conjugates to aza-dibenzocyclooctyne (ADIBO) gave the highest and most specific derivatization of azide-conjugated LAP in cells, and optimized two-step enzymatic/chemical labeling scheme was used to tag and image a variety of LAP fusion proteins in multiple mammalian cell lines with diverse fluorophores.
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Enantioselective total synthesis of (-)-acetylaranotin, a dihydrooxepine epidithiodiketopiperazine.

TL;DR: The first total synthesis of the dihydrooxepine-containing epidithiodiketopiperazine (ETP) (-)-acetylaranotin (1) is reported and it is anticipated that the approach described herein will serve as a general strategy for the synthesis of additional members of thedihydro oxepine ETP family.