Facile synthesis of caerulomycin e by the formation of 2, 2′-bipyridine core via a 2-pyridyl substituted 4H-pyran-4-one.Formal synthesis of caerulomycin A

Tetrahedron

Volumn 66, Issue 29, 2010, Pages 5432-5434

  Bobrov, Denis N ^a   Tyvorskii, Vladimir I ^b  

^a Oasmia Pharmaceutical AB   (Sweden)

^b BELARUSIAN STATE UNIVERSITY   (Belarus)

Author keywords

2,2 Bipyridines; 4H Pyran 4 ones; Caerulomycins; Claisen condensation

Indexed keywords

2,2' BIPYRIDINE; 4 ETHOXY 3 PENTEN 2 ONE; 6 METHYL 2 (2 PYRIDYL) 4H PYRAN 4 ONE; ACETYLACETONE; CAERULOMYCIN E; CERULOMYCIN; ETHER; NATURAL PRODUCT; PICOLINIC ACID; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CLAISEN CONDENSATION; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 77954314375     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.05.024     Document Type: Article

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