SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 9, 2011, Pages 3170-3175

Unprecedented stereoselective synthesis of cyclopenta[b]benzofuran derivatives and their characterisation assisted by aligned media NMR and 13C chemical shift ab initio predictions

(6) Riveira, Martín J a Gayathri, Chakicherla b Navarro Vázquez, Armando c Tsarevsky, Nicolay V d Gil, Roberto R b Mischne, Mirta P a

a Universidad Nacional de Rosario (Argentina)

b CARNEGIE MELLON UNIVERSITY (United States)

c UNIVERSITY OF VIGO (Spain)

d SOUTHERN METHODIST UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AB INITIO; AB INITIO PREDICTION; BENZOFURANS; CHARACTERISATION; DICARBONYL COMPOUNDS; NEW APPROACHES; NEW PRODUCT; NMR CHEMICAL SHIFTS; RESIDUAL DIPOLAR COUPLINGS; STEREOSELECTIVE SYNTHESIS; UNSATURATED ALDEHYDES;

ALDEHYDES; CHEMICAL SHIFT; FORECASTING; STEREOSELECTIVITY; UNSATURATED COMPOUNDS;

SYNTHESIS (CHEMICAL);

BENZOFURAN DERIVATIVE; CARBON;

ARTICLE; BIOLOGY; CHEMICAL STRUCTURE; CYCLIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

BENZOFURANS; CARBON ISOTOPES; COMPUTATIONAL BIOLOGY; CYCLIZATION; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 79954441931 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c1ob05109a Document Type: Article

Times cited : (27)

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