SYNTHESIS OF NEW HOMODRIMANE SESQUITERPENOIDS CONTAINING DIAZINE, 1,2,4-TRIAZOLE AND CARBAZOLE RINGS

Dragalin, Ion; Duca, Gheorghe; Gutu, Yacob; Tenu, Nadejda; Aricu, Aculina; Barba, Alic; Lungu, Lungu; Ciocarlan, Alexandru

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dc.contributor.author	Duca, Gheorghe
dc.contributor.author	Aricu, Aculina
dc.contributor.author	Lungu, Lungu
dc.contributor.author	Tenu, Nadejda
dc.contributor.author	Ciocarlan, Alexandru
dc.contributor.author	Gutu, Yacob
dc.contributor.author	Dragalin, Ion
dc.contributor.author	Barba, Alic
dc.date.accessioned	2019-02-19T14:24:38Z
dc.date.available	2019-02-19T14:24:38Z
dc.date.issued	2018
dc.identifier.citation	GUȚU, Ia. et al. Synthesis of new homodrimane sesquiterpenoids containing diazine, 1,2,4-triazole and carbazole rings. In: Cemistry Journal of Moldova. 2018, nr.1, pp. 69-73. ISSN 1857-1727.	en
dc.identifier.issn	1857-1727
dc.identifier.uri	http://dspace.usm.md:8080/xmlui/handle/123456789/1958
dc.description.abstract	The present paper reports on six step synthesis of 11-homodrim-6,8-dien-12-oic acid N-substituted amides containing diazine, 1,2,4-triazole and carbazole rings based on commercially available sclareolide. The mentioned compounds were prepared for the first time by interaction of the generated in situ acyl chloride with some heterocyclic amines: 2- and 4-aminopyrimidine, 2-aminopyrazine, 5-amino-1,2,4-triazole and N-aminocarbazole. Their structures were fully elucidated by elemental and spectral analyses (IR, 1H and 13C NMR).	en
dc.language.iso	en	en
dc.subject	N-substituted amide	en
dc.subject	heterocyclic amine	en
dc.subject	diazine	en
dc.subject	1,2,4-triazole	en
dc.subject	carbazole	en
dc.subject	sesquiterpenoid	en
dc.subject	synthesis	en
dc.title	SYNTHESIS OF NEW HOMODRIMANE SESQUITERPENOIDS CONTAINING DIAZINE, 1,2,4-TRIAZOLE AND CARBAZOLE RINGS	en
dc.type	Article	en