Highly selective synthesis of tricyclic compounds from semithioglycoluril, formaldehyde and amines

Highly selective synthesis of tricyclic compounds from semithioglycoluril, formaldehyde and amines Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2019, Volume: 29, Number: 3, Pages: 323-325 Pages count : 3 DOI: 10.1016/j.mencom.2019.05.028

Authors

Baranov Vladimir V. ¹ , Barsegyan Yana A. ¹ , Kolotyrkina Natalya G. ¹ , Kravchenko Angelina N. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

A highly selective one-pot synthesis of new 6-substituted 4-thioxohexahydro-5H-2,3,4a,6,7a-pentaazacyclopenta[cd]inden-1(2H)-ones by cycloaminomethylation of semithioglycolurile with formaldehyde and amines is proposed. A mechanism for the process is suggested.

Baranov V.V. , Barsegyan Y.A. , Kolotyrkina N.G. , Kravchenko A.N.
Highly selective synthesis of tricyclic compounds from semithioglycoluril, formaldehyde and amines
Mendeleev Communications. 2019. V.29. N3. P.323-325. DOI: 10.1016/j.mencom.2019.05.028 WOS Scopus OpenAlex

Web of science:	WOS:000472703800028
Scopus:	2-s2.0-85066872273
OpenAlex:	W2957177024

DB	Citing
OpenAlex	7
Scopus	7