Enzyme-Catalyzed\nRegioselective Synthesis of 4‑Hetero-Functionalized\n1,5-Disubstituted 1,2,3-Triazoles

Enzyme-catalyzed novel protocols for the regioselective\nconstruction\nof fully substituted 1,2,3-triazoles by employing 2-azido-1,3,5-triazine\n(ADT) as a 1,3-dipole for the cycloaddition reaction with the activated\nalkene in an aqueous medium have been developed. Various 4-heterosubstituted-1,2,3-triazoles\nwere readily assembled in good to excellent yields with high regioselectivity.\nThis reaction also features wide substrate scope, strong functional\ngroup tolerance, gram-scale synthesis, and an environmentally friendly\nprocess.

Publication Details

Journal
Figshare
Published
2024-09-04
DOI
https://doi.org/10.1021/acs.orglett.4c02341.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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article

Enzyme-Catalyzed\nRegioselective Synthesis of 4‑Hetero-Functionalized\n1,5-Disubstituted 1,2,3-Triazoles

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Mycorrhizal Fungi and Plant Interactions
article

Enzyme-Catalyzed\nRegioselective Synthesis of 4‑Hetero-Functionalized\n1,5-Disubstituted 1,2,3-Triazoles

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Abstract

Enzyme-catalyzed novel protocols for the regioselective\nconstruction\nof fully substituted 1,2,3-triazoles by employing 2-azido-1,3,5-triazine\n(ADT) as a 1,3-dipole for the cycloaddition reaction with the activated\nalkene in an aqueous medium have been developed. Various 4-heterosubstituted-1,2,3-triazoles\nwere readily assembled in good to excellent yields with high regioselectivity.\nThis reaction also features wide substrate scope, strong functional\ngroup tolerance, gram-scale synthesis, and an environmentally friendly\nprocess.

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Enzyme-Catalyzed\nRegioselective Synthesis of 4‑Hetero-Functionalized\n1,5-Disubstituted 1,2,3-Triazoles · Figshare (2024) | TGRS Research Map | TGRS