Drupal-Biblio17<style face="normal" font="default" size="100%">Catalytic transesterification of beta-ketoesters with zeolite H-FER under solvent free conditions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diastereoselective amidoalkylation of (3S,7aR)-6-benzyl-7-hydroxy-3-phenyltetra-hydro-5H-imidazo[1,5-c][1, 3]thiazol-5-one : a short and highly efficient synthesis of (+)-biotin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient stereoselective synthesis of (2S,4S,5R)-(-)- and (2R,4R,5S)-(+)-bulgecinine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile regioselective decomposition of tosylhydrazones: an application towards the synthesis of alpha-lipoic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (+)-beta-herbertenol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple, concise, stereocontrolled synthesis of (8E,10Z)-pentadecadien-1-ol acetate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simplistic expedient and practical synthesis of (+/-)-alpha-lipoic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of (-)-microcarpalide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of (+)-camptothecin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unusual stereochemical outcome of radical cyclization: synthesis of (+)-biotin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (-)-parvifoline and (-)-curcuquinone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ring closing metathesis approach to the indole alkaloid mitralactonine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Convenient formal synthesis of (+/-)-paroxetine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and practical total synthesis of (+/-)-alpha-cuparenone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile total synthesis of (+/-)-alpha-cuparenone employing diallylation and RCM as key steps</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (-)-heritol: absolute configuration determination</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MgBr2-mediated ionic Diels-Alder reaction of acetals of alpha,beta-unsaturated aldehydes and ketones with 1,3-dienes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Practical and facile approach towards indole alkaloids: (-)-mitralactonine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Practical formal synthesis of camptothecin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Practical synthesis of (+/-)-venlafaxine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short and efficient synthesis of rubrolide E</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+)-camptothecin via an intramolecular palladium-catalyzed cyclization strategy</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of pulchellalactam via an RCM strategy</style>Drupal-Biblio17<style face="normal" font="default" size="100%">ORGN 511-Total synthesis of 7-chloro-10-methoxycamptothecin: an important synthon for commercially important derivatives of camptothecin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tandem aza-michael-condensation-aldol cyclization reaction: approach to the construction of DE synthon of (+/-)-camptothecin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic enantioselective synthesis of beta-blockers: (S)-propranolol and (S)-naftopidil</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (R)-(+)-alpha-lipoic acid via proline-catalyzed sequential alpha-aminoxylation and HWE olefination of aldehyde</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fluconazole analogues containing 2H-1,4-benzothiazin-3(4H)-one or 2H-1,4-benzoxazin-3(4H)-one moieties, a novel class of anti-Candida agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (+/-)-camptothecin via tricyclic lactone as key synthon</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic asymmetric synthesis of (-)-delta-coniceine based on sequential proline-catalyzed asymmetric alpha-amination-HWE olefination</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric total synthesis of (2S,3S)-3-hydroxypipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Convenient formal synthesis of (2S,3S)-3-hydroxy pipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exploration of L-proline-catalyzed -aminoxylation of aldehyde to (S)-guaifenesin-related drug molecules</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel hybrids of fluconazole and furanones: design, synthesis and antifungal activity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-step synthesis of 4-alkyl-3-aryl-2,6-dicyanoanilines and their use in the synthesis of highly functionalized 2,3,5,6,7-and 2,3,4,5,7-substituted indoles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of the essential oil and pheromonal component ar-himachalene by a chiral pool and chirality induction approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (-)-stemoamide using a useful epimerization at C-8</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly diastereoselective total synthesis of (+/-)-heritonin and (+/-)-heritol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Very practical and selective method for PMB protection of alcohols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-pot migration-formylation of benzyl aryl ethers under duff reaction condition</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-step method for the synthesis of aryl olefins from aryl aldehydes and aliphatic aldehydes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short synthesis of (2S,3S)-3-hydroxypipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple synthesis of the novel antihistaminic drug olopatadine hydrochloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chiron approach to formal synthesis of both antipodes of cis 3-hydroxypipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and mild method for preparation of allylic amines from aziridine-2-alcohols using PPh3/I-2/imidazole</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile and convenient synthesis of (+/-)-Biotin via MgCl2/Et3N-mediated C-C coupling and mitsunobu reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel, concise and efficient protocol for non-natural piperidine compounds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Protecting group free and scalable approach towards total synthesis of (-)-venlafaxine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short enantioselective total synthesis of (R)- and (S)-pipecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereospecific synthetic approach towards tamiflu using the ramberg-backlund reaction from cysteine hydrochloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total syntheses of D-allo-1-deoxynojirimycin and L-talo-1-deoxynojirimycin via reductive cyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unusual, selective, reductive, deoxygenation of cyclopentenone alcohols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chirality induction and chiron approaches to enantioselective total synthesis of alpha-lipoic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective syntheses of (R)-pipecolic acid, (2R,3R)-3-hydroxypipecolic acid, beta-(+)-conhydrine and (-)-swainsonine using an aziridine derived common chiral synthon</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal syntheses of (2R,3R)-3-hydroxy pipecolic acid and (2R,3S)-3-hydroxy pipecolic acid from L-ascorbic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of 3-ethyl-4-metyl-1h,5-dihydro-2h-pyrrol-2-one by novel palladium(ii)-catalyzed cyclization and ring-closing metathesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (R)-lipoic acid and (S)-lipoic acid via an Mn (III)-salen-catalyzed oxidative kinetic resolution</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric total synthesis of L-allo-1-deoxynojirimycin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exploration of the diastereoselectivity in an unusual Grignard reaction and its application towards the synthesis of styryl lactones 7-epi-(+)-goniodiol and 8-epi-(-)-goniodiol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Application of unusual grignard reaction for the stereoselective synthesis of antidepressant drug (R)-(-)-venlafaxine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hybrids of thienopyrimidinones and thiouracils as anti-tubercular agents: SAR and docking studies</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and cell imaging applications of fluorescent mono/di/tri-heterocycl- yl-2,6-dicyanoanilines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of 3-azidopiperidine skeleton employing ceric ammonium nitrate (CAN)-mediated regioselective azidoalkoxylation of enol ether: total synthesis of d-2 receptor agonist (+/-)-quinagolide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective formal total synthesis of (-)-quinagolide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of brivaracetam: a key to construct the pyrrolidone scaffold using Pd-catalyzed oxidative cyclization and ring-closing metathesis reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+/-)-quinagolide: a potent D-2 receptor agonist for the treatment of hyperprolactinemia</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chiron approach to formal synthesis of both antipodes of cis 3-hydroxypipecolic acid (vol 55, pg 6423, 2014)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enolate-mediated regioselective synthesis of 1,2,3-triazoles via azide-aldehydes or ketones [3+2]-cycloaddition reactions in aqueous phase</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Furan-derived chiral bicycloaziridino lactone synthon: collective syntheses of oseltamivir phosphate (Tamiflu), (S)-pipecolic acid and its 3-hydroxy derivatives</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Scalable synthesis of 3-Ethyl-4-methyl-1,5-dihydro-2H-pyrrol-2-one: an important building block of the antidiabetic drug glimepiride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Application of allylic amine formation from aziridine-2-ol under appel reaction condition: synthesis of N-(tert-butoxycarbonyl)-D-vinyl glycine methyl ester</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Divergent approach to the synthesis of (-)-balanol heterocycle and cis-3-hydroxypipecolic acid based on chiral 2-aminoalkanol equivalent</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (-)-quinagolide: diastereoselective ring expansion via a bicyclic aziridinium ion strategy to access the octahydrobenzo[g]quinoline architecture</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-step synthesis of miltefosine: integration of flow chemistry with continuous mechanochemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and cell imaging applications of fluorescent mono/di/tri-heterocyclyl-2,6-dicyanoanilines (vol 27, pg 979, 2017)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">cis-aziridine synthon based synthetic investigation for tamiflu employing horner-wadsworth-emmons reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rapid synthesis of the epi-biotin sulfone via tandem S,N-carbonyl migration/aza-michael/spirocyclization and haller-bauer reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Revisiting classical pummerer cyclization reaction: a key strategy for the synthesis of (+/-)-quinagolide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rapid bioinspired N-acyliminium ion strategy for the ABC core of the stemona alkaloids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal Synthesis of Corynanthe Indole Alkaloid (±)-Mitralactonine: Construction of α-Hydroxy-Keto Functionalized Tetracyclic Skeleton</style>