Synthesis of novel polyfunctional pyrrolo[2,1-a]isoquinolines based on 1,3-dipolar cycloaddition reactions Full article
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Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Output data | Year: 2019, Volume: 68, Number: 9, Pages: 1729-1734 Pages count : 6 DOI: 10.1007/s11172-019-2617-x | ||
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Abstract:
A series of 5-substituted 8-nitroisoquinolines was synthesized based on the reaction of 5-bromo-8-nitroisoquinohne with various nucleophiles. N-Alkylation products of 8-nitroisoquinolines were shown to undergo 1,3-dipolar cycloaddition to substituted alkenes and alkynes as dipolarophiles in the presence of a base to form new polyfunctional nitro-containing pyrrolo-[2,1-a]isoquinolines and their hydrogenated analogs.
Cite:
Bastrakov M.A.
, Starosotnikov A.M.
Synthesis of novel polyfunctional pyrrolo[2,1-a]isoquinolines based on 1,3-dipolar cycloaddition reactions
Russian Chemical Bulletin. 2019. V.68. N9. P.1729-1734. DOI: 10.1007/s11172-019-2617-x WOS Scopus OpenAlex
Synthesis of novel polyfunctional pyrrolo[2,1-a]isoquinolines based on 1,3-dipolar cycloaddition reactions
Russian Chemical Bulletin. 2019. V.68. N9. P.1729-1734. DOI: 10.1007/s11172-019-2617-x WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000489761800013 |
| Scopus: | 2-s2.0-85073262155 |
| OpenAlex: | W2978976516 |