Intramolecular photoreactions of thiohomophthalimides with an alkenyl group in their  N ‐Side chain. Regioselective synthesis of heterocycle‐fused isoquinoline derivatives through [2+2] photocycloaddition | Zendy

Takechi Haruko | Zendy; Takahashi Hajime | Zendy; Machida Minoru | Zendy

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Intramolecular photoreactions of thiohomophthalimides with an alkenyl group in their N ‐Side chain. Regioselective synthesis of heterocycle‐fused isoquinoline derivatives through [2+2] photocycloaddition

Author(s) -

Takechi Haruko,

Takahashi Hajime,

Machida Minoru

Publication year - 2005

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.5570420204

Subject(s) - chemistry , isoquinoline , regioselectivity , intramolecular force , cycloaddition , side chain , stereochemistry , group (periodic table) , chain (unit) , medicinal chemistry , intramolecular reaction , organic chemistry , catalysis , polymer , physics , astronomy

Upon irradiation, thiohomophthalimides with an alkenyl group in their N ‐side chain or at the benzylic position give tricyclic isoquinoline derivatives through regioselective intramolecular [2+2] cycloaddition or Norrish type II reaction, respectively, in good yields.

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