A new general synthesis of functionally substituted pyrazolo[1,5-a]pyrimidines Full article
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Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Output data | Year: 2019, Volume: 29, Number: 4, Pages: 429-431 Pages count : 3 DOI: 10.1016/j.mencom.2019.07.025 | ||
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Abstract:
5,7-Dimethyl-2,3-dinitropyrazolo[1,5-a]pyrimidine in reaction with N-, S- and O-nucleophiles under mild conditions undergoes regioselective nucleophilic substitution of the 2-positioned nitro group, which provides an access to a library of 2-R-3-nitropyrazolo[1,5-a]pyrimidines.
Cite:
Shkineva T.K.
, Vatsadze I.A.
, Dalinger I.L.
A new general synthesis of functionally substituted pyrazolo[1,5-a]pyrimidines
Mendeleev Communications. 2019. V.29. N4. P.429-431. DOI: 10.1016/j.mencom.2019.07.025 WOS Scopus OpenAlex
A new general synthesis of functionally substituted pyrazolo[1,5-a]pyrimidines
Mendeleev Communications. 2019. V.29. N4. P.429-431. DOI: 10.1016/j.mencom.2019.07.025 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:000484653500025 |
| ≡ Scopus: | 2-s2.0-85070570699 |
| ≡ OpenAlex: | W2967994800 |