TY - JOUR
T1 - Denitrogenative Transformations of Pyridotriazoles and Related Compounds
T2 - Synthesis of N-Containing Heterocyclic Compounds and beyond
AU - Yadagiri, Dongari
AU - Rivas, Mónica
AU - Gevorgyan, Vladimir
N1 - Funding Information:
We thank the National Institute of Health (GM120281), National Science Foundation (CHE-1955663), and Welch Foundation (Chair, AT-0041) for financial support.
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/9/4
Y1 - 2020/9/4
N2 - The high demand for new and efficient routes toward synthesis of nitrogen-containing heterocyclic scaffolds has inspired organic chemists to discover several methodologies over recent years. This Perspective highlights one standout approach, which involves the use of pyridotriazoles and related compounds in denitrogenative transformations. Readily available pyridotriazoles undergo ring-chain isomerization to produce uniquely reactive α-diazoimines. Such reactivity, enabled by metal catalysts, additives, or visible-light irradiation, can be applied in transannulation, insertion, cyclopropanation, and many other transformations.
AB - The high demand for new and efficient routes toward synthesis of nitrogen-containing heterocyclic scaffolds has inspired organic chemists to discover several methodologies over recent years. This Perspective highlights one standout approach, which involves the use of pyridotriazoles and related compounds in denitrogenative transformations. Readily available pyridotriazoles undergo ring-chain isomerization to produce uniquely reactive α-diazoimines. Such reactivity, enabled by metal catalysts, additives, or visible-light irradiation, can be applied in transannulation, insertion, cyclopropanation, and many other transformations.
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U2 - 10.1021/acs.joc.0c01652
DO - 10.1021/acs.joc.0c01652
M3 - Review article
C2 - 32786635
AN - SCOPUS:85092132259
SN - 0022-3263
VL - 85
SP - 11030
EP - 11046
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 17
ER -