An inverse electron-demand diels-alder-based total synthesis of urolithin M7

Synlett

Volumn , Issue 15, 2011, Pages 2245-2247

  Pottie, Ian R ^a,b   Nandaluru, Penchal Reddy ^a   Bodwell, Graham J ^a  

^a MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^b MOUNT SAINT VINCENT UNIVERSITY   (Canada)

Author keywords

dibenzopyranone; domino reaction; inverse electron demand Diels Alder; urolithin M7

Indexed keywords

2 HYDROXY 4 METHOXYBENZALDEHYDE; 6H DIBENZO[B,D]PYRAN 6 ONE; ACETALDEHYDE; ALKADIENE; BENZALDEHYDE DERIVATIVE; ELLAGIC ACID; ELLAGITANNIN; ENAMINE; PYRAN DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG; UROLITHIN M7;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DIELS ALDER REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 80052670728     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1261203     Document Type: Article

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