Drupal-Biblio17<style face="normal" font="default" size="100%">Concise account of recent S(N)2 ` grignard coupling reactions in organic synthesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile synthesis of rubrolide E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple synthesis of (+/-)-sarkomycin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of naturally occurring bioactive butyrolactones: maculalactones A-C and nostoclide I</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemistry of recently isolated naturally occurring quinazolinone alkaloids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient amano PS-catalyzed chemo-, regio- and enantioselective hydrolysis of (+/-)-2,3-di-O-acetyl-2-C-methyl-D-erythrono-1,4-lactone: a facile preparation of bioactive natural products (-)-saccharinic acid lactone and potassium (2R,3R)-2,3,4-trihydr</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile synthesis of 1,3,7-trihydroxyxanthone and its regioselective coupling reactions with prenal: simple and efficient access to osajaxanthone and nigrolineaxanthone F</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile two-step chemoenzymatic access to natural germination inhibitor (+)-erigeronic acid A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Haval-Argade contrathermodynamic rearrangement of alkylidenesuccinimides to alkylmaleimides via the corresponding isoimides: a general approach to alkyl and dialkyl substituted maleimides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile chemo-, regio-, and diastereoselective approach to cis-3,5-disubstituted gamma-butyrolactones and fused gamma-butyrolactones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile phenol-driven intramolecular diastereoselective thermal/base-catalyzed dipolar [2+2] annulation reactions: an easy access to complex bioactive natural and unnatural benzopyran congeners</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile S(N)2 ' coupling reactions of wittig reagents with dimethyl bromomethylfumarate: synthesis of enes, dienes, and related natural products</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hexamethyldisilazane-iodine induced intramolecular dehydrative cyclization of diamides: a general access to natural and unnatural quinazolinones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Reactions of o-aminothiophenol and o-aminophenyl disulfide with itaconic anhydride and (-)-dimenthyl itaconate: access to enantiomerically pure 1,5-benzothiazepines and benzothiazolyl-2-methylacrylic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of natural fimbrolides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile air-oxidation of N-homopiperonyl-5,6-dimethoxyhomophthalimide: simple and efficient access to nuevamine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile biogenetic synthesis of pulcheotine A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General strategy for the synthesis of natural and unnatural dialkylmaleic anhydrides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of gymnoascolide A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of norpandamarilactonines, pandamarilactonines, and pandanamine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile approach to diverse range of 1,3-diaza-heterocycles: angular/linear selectivity paradigm and a remarkable intramolecular methyl migration</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of (+)-isoindolo-beta-carboline</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of the reported protoberberine gusanlung D</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+/-)-1,3,4,5-tetragalloylapiitol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Bromine-induced facile synthesis of butenolides and spirobutenolides from sterically congested tetrasubstituted dialkyl alkylidene succinates</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemoselective coupling reactions of 5,7-dimethoxyphthalide with the remotely functionalized alkyl iodides: facile racemic synthesis of helicobacter pylori antibiotics</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Copper-catalyzed intramolecular N-arylation of quinazolinones: facile convergent approach to (-)-circumdatins H and J</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General approach to 2,4-dialkyl-3-carboxybutyrolactones: an efficient synthesis of (+/-)-striatisporolide A and (+/-)-lichesterinic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of proposed auranthine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemoenzymatic total synthesis of potent HIV RNase H inhibitor (-)-1,3,4,5-tetragalloylapiitol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient convergent access to spiroketal segment of (+)-spiroxaline methyl ether</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Intramolecular chemoselective acylation of a suitably substituted isoindole: synthesis of (+/-)-chilenine and (+/-)-deoxychilenine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Regio- and stereoselective selenium dioxide allylic oxidation of (E)-dialkyl alkylidenesuccinates to (Z)-allylic alcohols: synthesis of natural and unnatural butenolides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Regioselective monoalkylation of dimethyl alkylidenesuccinates: simple approach to dialkyl-substituted maleic anhydrides including chaetomellic acid A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Regioselective NaBH4 and DIBAL-H reductions of 3,4-dimethoxyhomopiperonylphthalimide: concise and efficient synthesis of nuevamine and isonuevamine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile synthesis of oxyavicine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Palladium-catalyzed routes to geranylated or farnesylated phenolic stilbenes: synthesis of pawhuskin C and schweinfurthin J</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sonogashira coupling reactions of bromomaleimides: route to alkyne/cis-Alkene/Alkyl maleimides: synthesis of luffarin X and cacospongionolide C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthetic studies towards NG-121: diastereoselective synthesis of NG-121 methyl ether</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Aryne insertion reactions leading to bioactive fused quinazolinones: diastereoselective total synthesis of cruciferane</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Biology-orientated synthesis of putrescine bisamides gigantamide A, dasyclamide, and cucullamide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective total synthesis of desbromoarborescidines A-C and the formal synthesis of (S)-deplancheine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Palladium-promoted [2+2+2] cocyclization of arynes and unsymmetrical conjugated dienes: synthesis of justicidin B and retrojusticidin B</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Reactivity umpolung in intramolecular ring closure of 3,4-disubstituted butenolides: diastereoselective total synthesis of paeonilide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Base-stimulated 1,2-, 1,4-, and 1,6-eliminations in suitably substituted alkylidenesuccinates leading to natural and unnatural conjugated alkenyl(methyl)maleic anhydrides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise account of the chemistry of valuable alkyl(methyl)maleic anhydrides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dimethyl homophthalates to naphthopyrans: the total synthesis of arnottin I and the formal synthesis of (-)-arnottin II</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diversity oriented convergent access for collective total synthesis of bioactive multifunctional carbazole alkaloids: synthesis of carbazomycin A, carbazomycin B, hyellazole, chlorohyellazole, and clausenaline D</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile synthesis of the isoquinoline alkaloids doryanine and oxyhydrastinine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-catalyzed cross-coupling reactions of halomaleic anhydrides and halomaleimides: synthesis of structurally interesting and biologically important natural and unnatural products</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of chenopanone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (+)-harmicine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Biomimetic synthesis of phaitanthrin e involving a fragmentation of sp(3) carbon-carbon bond: synthesis and rearrangement of phaitanthrin D to phaitanthrin E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemoenzymatic collective synthesis of optically active hydroxyl(methyl)tetrahydronaphthalene-based bioactive terpenoids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sulfuryl chloride promoted gem-dichlorination-dehydrochlorination in alkyl benzothiazinylacetates: synthesis of the skeleton of trichochrome pigments</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of yangjinhualine A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Biomimetic collective total synthesis of bioactive carbazole alkaloids indizoline, mafaicheenamine A, claulamine A, claulansine A, and the proposed claulamine E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chemoenzymatic access to (+)-artabotriol and its application in collective synthesis of (+)-grandiamide D, (-)-tulipalin B, (+)-spirathundiol, and (+)-artabotriolcaffeate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of (-)-desethyleburnamonine, (-)-vindeburnol and (-)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (-)-phaitanthrin D and (+)-dihydropyrroloindoloquinazolinone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rearrangement of imine double bond in activated quinazolinones: synthesis of phaitanthrin E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of bioactive canthine alkaloid cordatanine comprising in situ double oxidative aromatization of tetrahydrocarbazole</style>
Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+/-)/(+)-subincanadine E and determination of absolute configuration</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diastereoselective synthesis of (A±)- epi-subincanadine C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of (+/-)-rhodoconferimide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Solid state auto-inversion of C-centrochirality: enantioselective total synthesis of furocarbazolones (-)-epi-claulansine D and (-)-claulansine D and pyranocarbazolone (+)-epi-claulansine C</style>