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Synthesis of 3-(5-amino-1H-1,2,4-triazol-3-yl)propanamides and their tautomerism

Digital Science - Figshare2026-03-27 更新2026-03-28 收录

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https://curate.curtin.edu.au/articles/journal_contribution/Synthesis_of_3-_5-amino-1H-1_2_4-triazol-3-yl_propanamides_and_their_tautomerism/31679083 数据链接链接失效反馈

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Synthesis of 3-(5-amino-1H-1,2,4-triazol-3-yl)propanamides and their tautomerism

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2026-03-27

合成化学

立体选择性环化

A novel protocol for the efficient preparation of α-hydroxy allylic thioesters via a Lewis base-catalyzed tandem isomerization/allylic alkylation process is reported. The resulting allylic thioesters

NIAID Data Ecosystem100

(Rax)-4-(((1R,2R)-2-Bromocyclohexyl)oxy)-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d1',2'-f][1,3,2]dioxaphosphepine 4-oxide (4.6)

合成化学

化合物表征

NMR, IR, HRMS, HPLC, and X-ray data for (Rax)-4-(((1R,2R)-2-bromocyclohexyl)oxy)-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d1',2'-f][1,3,2]dioxaphosphepine 4-oxide (4.6)

DataCite Commons2024-08-01 更新50

Nitroalkanes as Ketone Synthetic Equivalents in C–N and C–S Bond Formation Reactions

合成化学

极性反转反应

The umpolung strategy has been explored with 2-nitropropane derivatives featuring stabilized carbanion to latent ketone equivalents. The consequence of changing intrinsic polarity at the α-carbon of n

NIAID Data Ecosystem30

Scalable Sonochemical Synthetic Strategy for Pyrazolo[1,5‑ a ]pyridine Derivatives: First Catalyst-Free Concerted [3 + 2] Cycloaddition of Alkyne and Alkene Derivatives to 2‑Imino‑1 H ‑pyridin-1-amines

合成化学

吡唑并吡啶合成

A highly efficient and convenient one-pot sonochemical synthetic strategy has been sophisticated for synthesizing a novel class of polysubstituted pyrazolo[1,5-a]pyridines via [3 + 2] cycloaddition

NIAID Data Ecosystem60

2-isopropyl-5-methylphenyl docosanoate

合成化学

酯化反应产物

Reaction of thymol with lignoceric acid producing an off-white solid at room temperature. Suggested name for resulting ester: Thymyl lignocerate. NMR in deuterated trichloromethane. Impurities: Hexane

DataCite Commons2020-08-01 更新50

Synthesis of 3-(5-amino-1H-1,2,4-triazol-3-yl)propanamides and their tautomerism

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