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Design of 7-substituted 3-azabicyclo[3.3.1]non-6-enes based on allylboron-acetylene condensation Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2021, Volume: 70, Number: 10, Pages: 1987-1993 Pages count : 7 DOI: 10.1007/s11172-021-3306-0
Authors Iurenkov M.V. 1 , Potapova T.V. 1 , Baranin S.V. 1 , Bubnov Yu.N. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: An efficient synthesis of 7-substituted 3-azabicyclo[3.3.1]non-6-enes from available 3-borabicyclo[3.3.1]non-6-enes, the products of allylboron-acetylene condensation, was developed. The terminal alkynes with nitrogen-containing substituents were involved for the first time into the reaction with triallylborane.
Cite: Iurenkov M.V. , Potapova T.V. , Baranin S.V. , Bubnov Y.N.
Design of 7-substituted 3-azabicyclo[3.3.1]non-6-enes based on allylboron-acetylene condensation
Russian Chemical Bulletin. 2021. V.70. N10. P.1987-1993. DOI: 10.1007/s11172-021-3306-0 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000712972400015
≡ Scopus: 2-s2.0-85118241728
≡ OpenAlex: W3210544099
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