z-logo
Premium
Synthesis of the azocino[4,3‐ b ]indole core structure for the synthesis of strychnos alkaloids
Author(s) -
Ergün Yavuz,
Okay Gürol,
Patir Süleyman
Publication year - 2002
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570390212
Subject(s) - strychnos , chemistry , indole test , stereochemistry , total synthesis , combinatorial chemistry , alkaloid
The synthesis of compound 12 which has a hexahydro‐1,5‐methanoazocino[4,3‐ b ]indole structure for the synthesis of pentacyclic strychnos type alkaloids (tubifolin and tubifolidine) is described. Many new compounds 5–12 have also been synthesized.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here