Synthesis of 3-spiroannulated hexahydro-6,8a-epoxyisoquinolines

The title compounds were synthesised by the intramolecular [4+2]-cycloaddition of 1-N-furfurylamino-1-allylcyclanes in the presence of acetic anhydride.

Authors
Varlamov A.V. 1 , Nikitina E.V. 1 , Zubkov F.I. 1 , Shurupova O.V. 1 , Chernyshev A.I. 1
Editors
-
Journal
Mendeleev Communications
Publisher
Royal Society of Chemistry
Number of issue
1
Language
English
Pages
32-33
Status
Published
Department
-
Link
External link
DOI
10.1070/MC2002v012n01ABEH001535
Number
-
Volume
12
Year
2002
Organizations
  • 1 Department of Organic Chemistry, Peoples' Friendship Univ. of Russia, 117419 Moscow, Russian Federation
Keywords
1 n furfurylamino 1 allylcyclane derivative; 6,8a epoxyisoquinoline derivative; acetic anhydride; isoquinoline derivative; unclassified drug; article; chemical reaction; chemical structure; crystal structure; crystallization; derivatization; synthesis
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/226/