Research output: Contribution to journal › Article › peer-review
1,2,4-Triazines and Calcium Carbide in Catalyst-Free Synthesis of 2,3,6-Trisubstituted Pyridines and Their D-, 13C-, and Doubly D2-13C2-Labeled Analogues. / Воронин, Владимир Владимирович; Полынский, Михаил Вячеславович; Ледовская, Мария Сергеевна.
In: Chemistry - An Asian Journal, Vol. 18, No. 23, e202300781, 01.12.2023.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - 1,2,4-Triazines and Calcium Carbide in Catalyst-Free Synthesis of 2,3,6-Trisubstituted Pyridines and Their D-, 13C-, and Doubly D2-13C2-Labeled Analogues
AU - Воронин, Владимир Владимирович
AU - Полынский, Михаил Вячеславович
AU - Ледовская, Мария Сергеевна
PY - 2023/12/1
Y1 - 2023/12/1
N2 - A novel synthetic approach to 2,3,6-trisubstituted pyridines, their 4,5-dideuterated derivatives, 4,5-13C2- and doubly-labeled D2‑13C2-pyridines has been developed using catalyst-free [4+2] cycloaddition of 1,2,4-triazines and in situ generated acetylene or labeled acetylene. Calcium carbide and water or deuterium oxide were used for the in situ generation of acetylene and dideuteroacetylene. Calcium carbide-13C2 in the mixture with water or deuterium oxide was applied as 13C2-acetylene and D2-13C2-acetylene source.
AB - A novel synthetic approach to 2,3,6-trisubstituted pyridines, their 4,5-dideuterated derivatives, 4,5-13C2- and doubly-labeled D2‑13C2-pyridines has been developed using catalyst-free [4+2] cycloaddition of 1,2,4-triazines and in situ generated acetylene or labeled acetylene. Calcium carbide and water or deuterium oxide were used for the in situ generation of acetylene and dideuteroacetylene. Calcium carbide-13C2 in the mixture with water or deuterium oxide was applied as 13C2-acetylene and D2-13C2-acetylene source.
KW - ацетилен
KW - карбид кальция
KW - пиридин
KW - реакция Дильса-Альдера
KW - alkynes
KW - carbides
KW - cycloaddition
KW - isotopic labeling
KW - nitrogen heterocycles
UR - https://www.mendeley.com/catalogue/27eae0c8-016d-3cb3-ba78-20c0a57c8d29/
U2 - 10.1002/asia.202300781
DO - 10.1002/asia.202300781
M3 - Article
VL - 18
JO - Chemistry - An Asian Journal
JF - Chemistry - An Asian Journal
SN - 1861-4728
IS - 23
M1 - e202300781
ER -
ID: 113569274