Synthesis and NMR assignment of 1,4‐oxathiino[3,2‐ c ;5,6‐ c' ]diquinoline | Zendy

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Synthesis and NMR assignment of 1,4‐oxathiino[3,2‐ c ;5,6‐ c' ]diquinoline

Author(s) -

Pluta Krystian

Publication year - 1994

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.5570310252

Subject(s) - chemistry , yield (engineering) , ring (chemistry) , closure (psychology) , oxygen atom , atom (system on chip) , spectrum (functional analysis) , crystallography , computational chemistry , organic chemistry , molecule , physics , economics , market economy , quantum mechanics , computer science , thermodynamics , embedded system

1,4‐Oxathiinodiquinoline 3 was obtained in three ways from 1,4‐dithiinodiquinolines 1 and 2 via ring opening‐ring closure reactions with total yield of 19, 46 and 77%. Through‐space interactions between the H‐5 quinolinyl atoms and oxygen atom were discussed on the basis of 1 H nmr spectrum.

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