Pyrrolo[3,2‐ c ][1,2,5]benzotriazocine: A new ring system | Zendy

Passannanti Alessandra | Zendy; Diana Patrizia | Zendy; Barraja Paola | Zendy; Lauria Antonino | Zendy; Cirrincione Girolamo | Zendy; Mingoia Francesco | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Pyrrolo[3,2‐ c ][1,2,5]benzotriazocine: A new ring system

Author(s) -

Passannanti Alessandra,

Diana Patrizia,

Barraja Paola,

Lauria Antonino,

Cirrincione Girolamo,

Mingoia Francesco

Publication year - 1998

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.5570350655

Subject(s) - chemistry , ring (chemistry) , yield (engineering) , nucleophile , pyrrole , nucleophilic substitution , medicinal chemistry , series (stratigraphy) , stereochemistry , combinatorial chemistry , organic chemistry , catalysis , materials science , metallurgy , paleontology , biology

A nucleophilic substitution reaction in the pyrrole series, achieved by a neutral nucleophile, led to the key intermediate 7 which by reduction and successive diazotization afforded the new ring system pyrrolo[3,2‐ c ][1,2,5]benzotriazocine 9 in good yield.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research