Paper
Addition of 2-tert-butyldimethylsilyloxythiophene to activated quinones: an approach to thia analogues of kalafungin
Published Mar 27, 2006 · M. Brimble, Olivia Laita, J. E. Robinson
Tetrahedron
Q3 SJR score
18
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
2-tert-butyldimethylsilyloxythiophene can be used to synthesize thia analogues of the pyranonaphthoquinone antibiotic kalafungin, with BF3Et2O being the optimal catalyst.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Full text analysis coming soon...
References
Synthesis of pyrrolo[3,2-b]benzofurans and pyrrolo[3,2-b]naphthofurans via addition of a silyloxypyrrole to activated quinones
This study demonstrates a novel method for synthesizing pyrrolo[3,2-b]benzofurans and pyrrolo[3,2-b]naphthofurans, which can be used to create an aza-analogue of the pyranonaphthoquino
2004·27citations·M. Brimble et al.·Tetrahedron
Tetrahedron
InCl3-Catalyzed Tandem Michael/Friedel-Crafts Cyclization: A Novel Protocol for Chiral 2,4-Disubstituted Tetrahydroquinolines
InCl3-catalyzed tandem Michael/Friedel-Crafts cyclization provides a novel method for chiral 2,4-disubstituted tetrahydroquinolines with high stereoselectivity and good yields.
2004·16citations·J. Yadav et al.·Synthesis
Synthesis
Addition of pyrroles to electron deficient olefins employing InCl3
Pyrroles can be conjugated with electron-deficient olefins at ambient temperature to produce high-yield, selective Michael adducts without polymerization.
2001·53citations·J. Yadav et al.·Tetrahedron Letters
Tetrahedron Letters
Variable Strategy toward Carbasugars and Relatives. 1. Stereocontrolled Synthesis of Pseudo-β-d-gulopyranose, Pseudo-β-d-xylofuranose, (Pseudo-β-d-gulopyranosyl)amine, and (Pseudo-β-d-xylofuranosyl)amine
This study synthesized four novel, chiral nonracemic carbasugars using readily available heterocyclic diene scaffolds, expanding dienoxy silane chemistry's potential.
2000·29citations·G. Rassu et al.·Journal of Organic Chemistry
Journal of Organic Chemistry
The utility of furan-, pyrrole-, and thiophene-based 2-silyloxy dienes as demonstrated by modular synthesis of annonaceous acetogenin core units and their pyrrolidine and thiolane analogues.
This modular strategy effectively synthesizes annonaceous acetogenin core units and their analogues, resulting in structural diversity and a large number of isomeric isomers.
2000·25citations·F. Zanardi et al.·The Journal of organic chemistry
The Journal of organic chemistry
Synthetic studies toward pyranonaphthoquinone antibiotics
This study successfully synthesized the pyranonaphthoquinone antibiotic griseusin A, an analog of medermycin, and a dimeric pyranonaphthoquinone using a furofuran annulation/oxidative rearrangement strategy.
2000·19citations·M. Brimble·Pure and Applied Chemistry
Pure and Applied Chemistry
Lewis Acid Assisted Vinylogous Mannich and Mukaiyama Aldol Reactions: A Route to Densely Hydroxylated Indolizidine Alkaloid Analogues
This study presents a novel synthetic route to densely hydroxylated indolizidine alkaloid analogues using vinylogous Mannich and Mukaiyama aldol reactions, offering a promising strategy for synthesis of ring-B-expanded alexine-australine
1999·29citations·G. Rassu et al.·European Journal of Organic Chemistry
European Journal of Organic Chemistry
Citations
Synthesis and Photochemical Properties of Fluorescent Metabolites Generated from Fluorinated Benzoylmenadiones in Living Cells.
Fluorinated benzoylmenadiones (F-PDO) serve as a novel (pro)-fluorescent probe for monitoring redox processes and protein alkylation in living cells.
2023·2citations·Nathan Trometer et al.·The Journal of organic chemistry
The Journal of organic chemistry
New 2-Acetyl-3-aminophenyl-1,4-naphthoquinones: Synthesis and In Vitro Antiproliferative Activities on Breast and Prostate Human Cancer Cells
Two members of the 2-acyl-3-aminophenyl-1,4-naphthoquinone series showed interesting cytotoxic activities on human prostate and mammary cancer cells.
2020·5citations·David Ríos et al.·Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity
Lewis Acid‐Catalyzed Stereoselective α‐Addition of Chiral Aldehydes to Cyclic Dienol Silanes: Aqueous Synthesis of Chiral Butenolides
This study successfully synthesized six bioactive natural products using a novel catalytic Mukaiyama aldol addition method for chiral butenolides in water-containing solvents.
2020·3citations·A. Adamkiewicz et al.·Advanced Synthesis & Catalysis
Advanced Synthesis & Catalysis
A catalytic asymmetric one-pot [3+2] cyclization/semipinacol rearrangement sequence: an efficient construction of a multi-substituted 3H-spiro[benzofuran-2,1'-cyclopentane] skeleton.
This one-pot method efficiently creates chiral multi-substituted 3H-spiro[benzofuran-2,1'-cyclopentane] structures with excellent enantioselectivity and diastereoselectivity, offering an alternative strategy for synthesis of bio
2019·8citations·Lin Liu et al.·Chemical communications
Chemical communications
α-Regioselective Aqueous Mukaiyama Aldol Reaction of 2-(Trimethylsilyloxy)furan with Pyruvates
This study presents a method for -regioselective aldol reaction of O-silylated dienolates, enabling access to -(hydroxyalkyl)butenolides with excellent regiocontrol and enantioselectivity.
2016·6citations·A. Adamkiewicz et al.·European Journal of Organic Chemistry
European Journal of Organic Chemistry
Synthesis of novel and diverse naphtho[1,2-b]furans by phosphine-catalyzed [3+2] annulation of activated 1,4-naphthoquinones and acetylenecarboxylates
This study presents a facile and efficient method for synthesizing diverse novel naphtho[1,2-(b)]furans from 1,4-naphthoquinones, offering potential biological applications.
2014·7citations·L. Xia et al.·Molecular Diversity
Molecular Diversity
Regioselective synthesis of novel and diverse naphtho[1,2-b]furan-3-carboxamides and benzofuran-3-carboxamides by cascade formal [3 + 2] cycloaddition
This novel In(OTf)3-catalyzed cascade formal [3 + 2] cycloaddition method efficiently synthesizes novel and diverse naphtho[1,2-b]furan-3-carboxamides and benzofuran-3-carboxamides with high regio
2014·12citations·L. Xia et al.·RSC Advances
RSC Advances
A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin.
This novel approach enables the rapid synthesis of diverse dihydronaphtho[1,2-b]furans and the biologically important natural product furomollugin in only 2 steps.
2013·33citations·L. Xia et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry