Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric aminohydroxylation route to (+)-L-733,060</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric synthesis of (-)-alpha-conhydrine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric synthesis of both the enantiomers of trans-3-hydroxypipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric aminohydroxylation route to cis-2,6-disubstituted piperidine-3-ol: application to the synthesis of (-)-deoxocassine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric dihydroxylation route towards the synthesis of (R)-clorprenaline hydrochloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Application of hydrolytic kinetic resolution (HKR) in the synthesis of bioactive compounds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise synthesis of (-)-deoxoprosopinine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient total synthesis of (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (-)-pinellic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of herbarumin III</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple and efficient approach to 1,3-aminoalcohols: application to the synthesis of (+)-negamycin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chiral Mn(III) salen complex immobilized onto ionic liquid modified mesoporous silica for oxidative kinetic resolution of secondary alcohols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise synthesis of protected (2S,4R)-4-hydroxyornithine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dimethyl sulfoxide pivaloyl chloride: a new reagent for oxidation of alcohols to carbonyls</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient total synthesis of decarestrictine D</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective hydrogenation of olefins by chiral iridium phosphorothioite complex covalently anchored on mesoporous silica</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-component carbon-carbon bond forming Mannich reaction catalyzed by yttria-zirconia based Lewis acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of alpha-amino phosphonates by three component condensation of carbonyl compound, amine, and dialkyl phosphite using Yttria-zirconia based Lewis acid catalyst</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+)-isolaurepan</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of decarestrictine J</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile synthesis of 5,6-dihydro-5-hydroxy-2(1H)-pyridone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First asymmetric total synthesis of aspinolide A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General approach to medium-sized ring ethers via hydrolytic and oxidative kinetic resolutions: stereoselective syntheses of (-)-cis-lauthisan and (+)-isolaurepan</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hydrolytic kinetic resolution as an emerging tool in the synthesis of bioactive molecules</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Iterative approach to enantiopure syn/anti-1,3-polyols via proline-catalyzed sequential alpha-aminoxylation and horner-wadsworth-emmons olefination of aldehydes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel synthesis of coumarins employing triphenyl(alpha-carboxymethylene)-phosphorane imidazolide as a C-2 synthon</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Oxidative kinetic resolution of alcohols using chiral Mn-salen complex immobilized onto ionic liquid modified silica</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of chiral sulfoxides by enantioselective sulfide oxidation and subsequent oxidative kinetic resolution using immobilized Ti-binol complex</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tethered aminohydroxylation route to L-arabino-[2R,3S,4R] and L-xylo-[2R,3S,4S]-C-18-phytosphingosines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Yttria-zirconia-based lewis acid catalysis of the biginelli reaction: an efficient one-pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise synthesis of (2S,3S,4S)-2-(Hydroxymethyl)pyrrolidine-3,4-diol (LAB1)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantio- and diastereocontrolled total synthesis of (+)-strictifolione</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of syn/anti-1,3-amino alcohols via proline-catalyzed sequential alpha-aminoxylation/alpha-amination and horner-wadsworth-emmons olefination of aldehydes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General and concise asymmetric synthesis of sphingosine, safingol and phytosphingosines via tethered aminohydroxylation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly selective claisen-schmidt condensation catalyzed by silica chloride under solvent-free reaction conditions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic route to the synthesis of lactone moiety of compactin and mevinolin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pivaloyl chloride/DMF: a new reagent for conversion of alcohols to chlorides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short and efficient synthesis of (S)-(+)-2-(Hydroxymethyl)-6-piperidin-2-one</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of aculeatins A and B via iterative hydrolytic kinetic resolution</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (-)-galantinic acid via iterative hydrolytic kinetic resolution and tethered aminohydroxylation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (R)-coniine and (S)-coinicine via organocatalytic alpha-aminoxylation of an aldehyde</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric dihydroxylation route to (-)-bulgecinine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic enantioselective approach to the synthesis of verbalactone and (R)-massoialactone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic route to the synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one and ravensara lactones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of (-)-galantinic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of ophiocerins A and C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (R)-selegiline via hydrolytic kinetic resolution</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of seimatopolide B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of tetrahydrolipstatin and tetrahydroesterastin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic stereoselective synthesis of passifloricin A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric routes to pentadec-1-en-4-ol: application to the syntheses of aculeatins F and epi-F, (R)- and (S)-5-hexadecanolide and a formal synthesis of solenopsin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise synthesis of (5R,6S)-tert-butyl 5-acetoxy-6-(hydroxymethyl)-5,6-dihydropyridine-1(2H)-carboxylate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Desymmetrization approach to the enantiopure syn/anti-1,5-diols via hydrolytic kinetic resolution (hkr) of functionalized meso-bis-epoxides: further elaboration to syn/syn-1,3,5-triols and application to the formal synthesis of cryptocarya diacetate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly concise and practical route to clavaminols, sphinganine and (+)-spisulosine via indium mediated allylation of alpha-hydrazino aldehyde and a theoretical insight into the stereochemical aspects of the reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Proline catalyzed alpha-aminoxylation reaction in the synthesis of biologically active compounds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Proline-catalyzed asymmetric synthesis of syn- and anti-1,3-diamines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of indolizidine, pyrrolizidine and quinolizidine ring systems by proline-catalyzed sequential alpha-amination and HWE olefination of an aldehyde</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of umuravumbolide and hyptolide through silicon-tethered ring-closing metathesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemoselective deprotection of N-allylic amines using DDQ</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Clay-supported copper nitrate (Claycop): a mild reagent for the selective nitration of aromatic olefins</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Croncise organocatalytic route to protected (2S, 4R)-4-hydroxyornithine and(+)-pseudohygroline</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Flexible, polymer-supported synthesis of sphingosine derivatives provides ceramides with enhanced biological activity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic stereoselective approach to the total synthesis of (-)-halosaline</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective approach to 2,6-disubstituted piperidin-3-ol: synthesis of (-)-deoxoprosopinine and (+)-deoxoprosophylline</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective approach to indolizidine and pyrrolizidine alkaloids: total synthesis of (-)-lentiginosine, (-)-epi-lentiginosine and (-)-dihydroxypyrrolizidine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carbon-carbon bond forming reactions: application of covalently anchored 2,4,6-triallyloxy-1,3,5-triazine (TAT) Pd(II) complex over modified surface of SBA-15 to Heck, Suzuki, Sonogashira and Hiyama cross coupling reactions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dinuclear salen cobalt complex incorporating Y(OTf)(3): enhanced enantioselectivity in the hydrolytic kinetic resolution of epoxides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mild regiospecific alcoholysis and aminolysis of epoxides catalyzed by zirconium(IV) oxynitrate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Modular synthesis of biaryl-substituted phosphine ligands: application in microwave-assisted palladium-catalyzed C-N cross-coupling reactions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nucleophilic fluorination using imidazolium based ionic liquid bearing tert-alcohol moiety</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereocontrolled synthesis of Hagen's gland lactones via iterative proline catalyzed alpha-aminoxylation and oxa-Michael addition reactions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+)-petromyroxol via tandem alpha-aminoxylation-allylation and asymmetric dihydroxylation-S(N)2 cyclization approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">CeCl3 center dot 7H(2)O-NaI promoted regioselective sulfenylation of indoles with sulfonylhydrazides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective modular total synthesis of macrolides Sch725674 and C-4-epi-Sch725674</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of ophiocerins A, B and C, botryolide E, decarestrictine O, stagonolide C and 9-epi-stagonolide C employing chiral hexane-1,2,3,5-tetraol derivatives as building blocks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (-)-(6R,11R,14S)-colletallol via proline catalyzed alpha-aminoxylation and Yamaguchi macrolactonization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly active recyclable SBA-15-EDTA-Pd catalyst for Mizoroki-Heck, Stille and Kumada C-C coupling reactions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tf2NH-catalyzed 1,6-conjugate addition of vinyl azides with p-quinone methides: a mild and efficient method for the synthesis of β-bis-arylamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Transition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unified approach to fused and spirocyclic oxindoles through lewis-acid-promoted opening of spiroepoxyoxindoles with allylsilanes: application to the formal synthesis of (+/-)-physovenine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of the proposed structure of pandangolide 1</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Harnessing nucleophilicity of allenol ester with p-quinone methides via gold catalysis: application to the synthesis of diarylmethine-substituted enones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Proline-catalyzed asymmetric -amination in the synthesis of bioactive molecules</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of heterogeneous Ru(II)-1,2,3-triazole catalyst supported over SBA-15: application to the hydrogen transfer reaction and unusual highly selective 1,4-disubstituted triazole formation via multicomponent click reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unravelling the nucleophilicity of buten tides for 1,6-conjugate addition to p-quinone methides: a direct access to diversely substituted butenolide-derived diarylmethanes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Acidic handle assemble heterogeneous carbocatalyst for facile aliphatic nucleophilic fluorination</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Regioselective one-pot synthesis of 3-fluoro-imidazo[1,2-a]pyridines from styrene</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Retraction: organocatalytic stereoselective synthesis of passifloricin A (Retraction of Vol 10, Pg 1820, 2012)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tf2NH catalyzed 1,6-conjugate addition of 2-hydroxy-p-quinone methides with -functionalized ketones: access to 2,3,4,9-Tetrahydro-1H-xanthenones and 4H-Chromene Derivatives</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantio- and diastereocontrolled conversion of chiral epoxides to trans-cyclopropane carboxylates: application to the synthesis of cascarillic acid, grenadamide and L-(-)-CCG-II (vol 10, pg 6987, 2012)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General and concise asymmetric synthesis of sphingosine, safingol and phytosphingosines via tethered aminohydroxylation (vol 8, pg 5074, 2010)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (-)-2-methoxy-2-butenolide-3-cinnamate and its antimicrobial potentials</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free, Tf2NH-catalyzed 1, 6-conjugate addition of imidazopyridine to para-quinone methides: easy access to C3-functionalized triarylmethane imidazopyridine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic route to the enantioselective synthesis of syn/ anti-α-hydrazino-γ-fluoro alcohols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tetrahydrofuran ring construction through tandem iodocyclizations: synthesis of hagen's gland lactones, a pheromone of idea leuconoe , an oxylipid, and related compounds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">H5IO6, as an efficient reagent for the aromatization of tetrahydro-β-carbolines: total synthesis of norharman, harmane, harmine, kumujian-C, and orthoscuticellines B</style>