pallidol and indacrinone

pallidol has been researched along with indacrinone* in 1 studies

Other Studies

1 other study(ies) available for pallidol and indacrinone

Article	Year
Sulfoxide-Based Enantioselective Nazarov Cyclization: Divergent Syntheses of (+)-Isopaucifloral F, (+)-Quadrangularin A, and (+)-Pallidol. Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Oct-04, Volume: 22, Issue:41 The synthesis of enantiomerically pure 3-aryl substituted indanones is developed using an enantioselective sulfoxide-based Knoevenagel condensation/Nazarov cyclization procedure. After the reductive desulfonation of the methyl para-tolyl sulfoxide-containing chiral auxiliary under mild conditions, selected enantiomerically pure indanone is used for the divergent total syntheses of three resveratrol natural products (+)-isopaucifloral F, (+)-quadrangularin A, and (+)-pallidol. Topics: Biological Products; Cyclization; Indans; Molecular Structure; Polycyclic Compounds; Stereoisomerism; Stilbenes; Sulfoxides	2016

Article

Year

Sulfoxide-Based Enantioselective Nazarov Cyclization: Divergent Syntheses of (+)-Isopaucifloral F, (+)-Quadrangularin A, and (+)-Pallidol.

Chemistry (Weinheim an der Bergstrasse, Germany), 2016, Oct-04, Volume: 22, Issue:41

The synthesis of enantiomerically pure 3-aryl substituted indanones is developed using an enantioselective sulfoxide-based Knoevenagel condensation/Nazarov cyclization procedure. After the reductive desulfonation of the methyl para-tolyl sulfoxide-containing chiral auxiliary under mild conditions, selected enantiomerically pure indanone is used for the divergent total syntheses of three resveratrol natural products (+)-isopaucifloral F, (+)-quadrangularin A, and (+)-pallidol.

Topics: Biological Products; Cyclization; Indans; Molecular Structure; Polycyclic Compounds; Stereoisomerism; Stilbenes; Sulfoxides

2016