Studies on chalcogen-containing heterocycles. Part 38: Regio- and stereoselective tandem addition-iodocyclization of 2-ethynylphenyl isothiocyanates with N- and O-nucleophiles affording 4-(iodoalkylidene)benzo[d] [1,3]thiazines

Tetrahedron

Volumn 69, Issue 31, 2013, Pages 6478-6487

  Sashida, Haruki ^a   Kaname, Mamoru ^a   Minoura, Mao ^b  

^a HOKURIKU UNIVERSITY   (Japan)

^b KITASATO UNIVERSITY   (Japan)

Author keywords

1,3 Benzothiazine; 6 exo dig Mode; Iodocyclization; Isothiocyanate; Tandem addition cyclization

Indexed keywords

2 AMINO 4 (1 IODOMETHYLIDENE)BENZO[D][1,3]THIAZINE DERIVATIVE; AMINE; BENZOTHIAZINE DERIVATIVE; CHALCOGEN; HETEROCYCLIC COMPOUND; ISOTHIOCYANIC ACID DERIVATIVE; NUCLEOPHILE; OXIDE; PALLADIUM; THIOUREA; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CROSS COUPLING REACTION; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; ONE POT SYNTHESIS; PRIORITY JOURNAL; REACTION OPTIMIZATION; REACTION TIME; STEREOCHEMISTRY;

EID: 84879215240     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.069     Document Type: Article

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