Drupal-Biblio17<style face="normal" font="default" size="100%">First synthesis of a noreremophilane isolated from the roots of ligularia przewalskii</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mild and efficient method for the synthesis of vinylogous carbamates from alkyl azides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple procedure for the synthesis of gamma-hydroxy-alpha,beta-(E)-alkenoic esters: formal synthesis of (+)-macrosphelides A and B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of small cyclic peptides constrained with 3-(3-aminomethylphenyl)propionic acid linkers using free radical-mediated macrocyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise asymmetric route to the antibiotic macrolides patulolide A and pyrenophorin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of cyclic peptides using a palladium-catalyzed enyne cycloisomerization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New route to eremophilanes: synthesis of (+/-)-eremophilenolide, (+/-)-eremophiledinone, and (+/-)-deoxyeremopetasidione</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+/-)-petasitolone and (+/-)-fukinone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of varenicline</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiospecific synthesis of sex pheromone of the obscure mealybug from pantolactone via tandem conjugate addition/cyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiospecific route to (+)-(1R, 3S)-cis-chrysanthemic acid from (-)-D-pantolactone(1)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel pyrazole-3-carboxamide derivatives as cannabinoid-1 (CB1) antagonists: journey from non-polar to polar amides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Phosphine-mediated synthesis of 1,4-oxazepine- and 1,5-oxazocine-based sugar hybrids from deoxysugar azides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of molluscicidal agent cyanolide a macrolactone from D-(-)-pantolactone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of novel dihydrooxazine and oxazoline based sugar hybrids from sugar azides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of isofregenedadiol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Antituberculosis agent diaportheone B: synthesis, absolute configuration assignment, and anti-TB activity of its analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Green synthetic route to antimalarial and antibacterial agent CJ-15,801 and its isomer cis-CJ-15,801</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Studies toward the synthesis of potent anti-inflammatory peptides solomonamides A and B: synthesis of a macrocyclic skeleton and key fragment 4-amino-6-(2 `-amino-4 `-hydroxyphenyl)-3-hydroxy-2-methyl-6-oxohexanoic acid (AHMOA)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of isomeric corniculatolides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diverted total syntheses of potent cell adhesion inhibitor peribysin E analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiodivergent routes to (+) and (-)-novioses from (-)-pantolactone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of hunanamycin A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheses and determination of absolute configurations and biological activities of the enantiomers of the longtailed mealybug pheromone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of a sex pheromone of the longtailed mealybug, pseudococcus longispinus</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of palmyrolide A and its cis-isomer and mechanistic insight into trans-cis isomerisation of the enamide macrocycle</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Access to harmonine, a chemical weapon of ladybird beetles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efforts towards the synthesis of microsporin B: ready access to both the enantiomers of the key amino acid fragment</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General approach to N-heterocyclic carbenes with a fused tetracyclic core: ligands for suzuki-miyaura cross-coupling reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of an anticancer norsesquiterpene alkaloid isolated from the fungus flammulina velutipes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of deoxy-solomonamide B by mimicking biogenesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+/-)-nardoaristolone B and its analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Zinc mediated allylations of chlorosilanes promoted by ultrasound: synthesis of novel constrained sila amino acids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Breaking and making of olefins simultaneously using ozonolysis: application to the synthesis of useful building blocks and macrocyclic core of solomonamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Breaking and making of rings: a method for the preparation of 4-quinolone-3-carboxylic acid amides and the expensive drug ivacaftor</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis, and identification of silicon incorporated oxazolidinone antibiotics with improved brain exposure</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiospecific synthesis of both enantiomers of the longtailed mealybug pheromone and their evaluation in a new zealand vineyard</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First synthesis of nitrosporeusines, alkaloids with multiple biological activities</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Silicon incorporated morpholine antifungals: design, synthesis, and biological evaluation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of novel N-cyclopentenyl-lactams using the aube reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total syntheses and biological evaluation of (+/-)-botryosphaeridione, (+/-)-pleodendione, 4-epi-periconianone B, and analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis and structural revision of mycalol, an anticancer natural product from the marine source</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiospecific formal synthesis of inthomycin C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of gliomasolide C and formal total synthesis of sch-725674</style>Drupal-Biblio17<style face="normal" font="default" size="100%">GSH Induced controlled release of levofloxacin from a purpose-built prodrug: luminescence response for probing the drug release in escherichia coli and staphylococcus aureus</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of noreremophilane-based inhibitors of angiogenesis using zebrafish assays</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecules with O-acetyl group protect protein glycation by acetylating lysine residues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-gram scale synthesis of hunanamycin A, an antibiotic natural product from the marine source</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Repurposing of a drug scaffold: identification of novel sila analogues of rimonabant as potent antitubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Solution-phase synthesis of the macrocyclic core of teixobactin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and biological evaluation of palmyrolide a macrocycles as sodium channel blockers towards neuroprotection</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of revised structure of klaivanolide (acetylmelodorinol)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (-)-nardoaristolone B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of the marine natural product solomonamide B necessitates stereochemical revision</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Access to fused tricyclic gamma-butyrolactones, a natural product -like scaffold</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Determination of the absolute configuration of gliomasolide D through total syntheses of the C-17 epimers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification and synthesis of mycalol analogues with improved potency against anaplastic thyroid carcinonia cell lines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of new anti-inflammatory agents based on nitrosporeusine natural products of marine origin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Route to benzimidazol-2-ones via decarbonylative ring contraction of quinoxalinediones: application to the synthesis of flibanserin, A drug for treating hypoactive sexual desire disorder in women and marine natural product hunanamycin analogue</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of natural fregenedadiol and its diacetate, rearranged labdanes with aromatized B ring</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Evaluating antimalarial efficacy by tracking glycolysis in Plasmodium falciparum using NMR spectroscopy</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-step continuous flow synthesis of the cystic fibrosis medicine ivacaftor</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> Nitrosporeusine analogue ameliorates Chandipura virus induced inflammatory response in CNS via NF kappa b inactivation in microglia</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Quest for novel chemical entities through incorporation of silicon in drug scaffolds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Specific stereoisomeric conformations determine the drug potency of cladosporin scaffold against malarial parasite</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Targeted phenotypic screening in plasmodium falciparum and toxoplasma gondii reveals novel modes of action of medicines for malaria venture malaria box molecules</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis and biological evaluation of cell adhesion inhibitors peribysin A and B: structural revision of peribysin B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of an anticancer natural product (+/-)-peharmaline A and its analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of the potent anti-inflammatory natural product solomonamide A along with structural revision and biological activity evaluation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Access to a stereoisomer library of solomonamide macrocycles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neural anti-inflammatory natural product periconianone A: total synthesis and biological evaluation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Route to access imidazol[1,5-a]indole-1,3-diones and pyrrolo[1,2-c]imidazole-1,3-diones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Scalable synthesis of cladosporin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of chiral tetrahydrofuran building blocks from pantolactones: application in the synthesis of empagliflozin and amprenavir analogs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Targeted phenotypic screening in plasmodium falciparum and toxoplasma gondii reveals novel modes of action of medicines for malaria venture malaria box molecules (vol 3, e00534-17, 2018)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of Met(10)-teixobactin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">DFT/NMR approach for the configuration assignment of groups of stereoisomers by the combination and comparison of experimental and predicted sets of data</style>Drupal-Biblio17<style face="normal" font="default" size="100%">FeCl3-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Overturning the peribysin family natural products isolated from periconia byssoides OUPS-N133: synthesis and stereochemical revision of peribysins A, B, C, F, and G</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of alpha-ketoamides using potassium superoxide (KO2) as an oxidizing agent</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Teixobactin: a paving stone toward a new class of antibiotics?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis and absolute configuration determination of Ktedonoketone, a benzenoid metabolite from Thermophilic bacterium</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Biological process of lysine-tRNA charging is therapeutically targetable in liver cancer</style>Drupal-Biblio17<style face="normal" font="default" size="100%">DBU/O-2-mediated oxidation of dienones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Herbicidal bio-assay of isocladosporin enantiomers and determination of its plausible absolute configuration</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of a novel series of potent organosilicon mosquito repellents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-pot oxidation of secondary alcohols to alpha-hydroxy ketones: application to synthesis of oxoaplysinopsin D, E, F, & G</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Scalable, sustainable and catalyst-free continuous flow ozonolysis of fatty acids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Separation of a diastereomeric diol pair using the mechanical properties of crystals</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and biological evaluation of hoshionolactam-based compounds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of a hypothetical macroketone of migrastatin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of twelve membered resorcyclic acid lactones, (R)-penicimenolide A, (R)-resorcyclide and (R)-dihydroresorcyclide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tuning of alpha-silyl carbocation reactivity into enone transposition: application to the synthesis of peribysin D, E-volkendousin, and E-guggulsterone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Antibiotic natural product hunanamycin A: Lead identification towards anti-Salmonella agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Kupyaphores are zinc homeostatic metallophores required for colonization of Mycobacterium tuberculosis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Postmodification of voxelotor (GBT 440) via [Rh]-catalyzed cross dehydrogenative coupling with olefins br</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ready access to benzannulated [5,5]-oxaspirolactones using Au(III)-catalyzed cascade cyclizations</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ready access to densely substituted furans using Tsuji-Wacker type cyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of 12, 13-dibenzyl-banistenoside B and analogs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Comprehensive study on solomonamides: total synthesis, stereochemical revision, and SAR studies toward identification of simplified lead</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Developing a mealybug pheromone monitoring tool to enhance IPM practices in New Zealand vineyards</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Direct deoxygenation of α-hydroxy and α,β-dihydroxy ketones using a silyl lithium reagent</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of new modulator of DNA repairing pathways based on natural product (±)-peharmaline A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Scalable synthesis of silacyclohexanones and ready access to silicon building blocks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: an effective strategy towards development of potent anti-tubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis and absolute configuration determination of the α-glycosidase inhibitor (3S,4R)-6-Acetyl-3-hydroxy-2,2-dimethylchroman-4-yl (Z)-2-Methylbut-2-enoate from Ageratina grandifolia</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly stereoselective diels-alder-based strategy for the synthesis of 3-epi-formicin A and 1-epi-formicin B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of benzofuran-6-carboxylic acid, an intermediate of lifitegrast with low-carbon footprints</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis and revision of stereochemistry of a natural benzo[g]isochromene stereodiad isolated from rubia philippinensis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enzymatic pathway for kupyaphore degradation in mycobacterium tuberculosis: mechanism of metal homeostasis and turnover</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Gram-scale synthesis of (±)-tylophorine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Interplay between genotoxic stress and STING activation in cellular senescence and inflammatory responses</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Peganutonin A: computationally informed synthesis of its revised structure</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ready access to benzodiazocines from tryptamines: a druggable scaffold toward antiviral agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Scalable and sustainable reductive amidation of nitroarenes, nitroalkenes, and nitroalkyls with acyl saccharins in aqueous media</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Silicon incorporated tacrine: design, synthesis, and evaluation of biological and pharmacokinetic parameters</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel routes for bioproduction of delta lactone aroma compounds</style>