Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic activation of TMSCN by basic ammonium salts for efficient cyanation of aldehydes and imines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NaIO4-KI-NaN3 as a new reagent system for C-H functionalization in hydrocarbons</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise enantioselective synthesis of (+)-decarestrictine L via proline-catalyzed sequential alpha-aminooxylation and Horner-Wadsworth-Emmons olefination</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Titanium superoxide: a heterogeneous catalyst for anti-Markovnikov aminobromination of olefins</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Co(III)(salen)-catalyzed HKR of two stereocentered alkoxy- and azido epoxides: a concise enantioselective synthesis of (S,S)-reboxetine and (+)-epi-cytoxazone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile enantioselective synthesis of (S)-N-(5-chlorothiophene-2-sulfonyl)-beta,beta-diethylalaninol via proline-catalyzed asymmetric alpha-aminooxylation and alpha-amination of aldehyde</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NaIO4/LiBr-mediated aziridination of olefins using chloramine-T</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel synthesis and characterization of titanium superoxide and its application in organic oxidative processes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Regiospecific azidoiodination of alkenes with sodium periodate, potassium iodide, and sodium azide: a high-yield synthesis of beta-iodoazides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short enantioselective synthesis of guggultetrol, a naturally occurring lipid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise enantioselective synthesis of (+)-goniodiol and (+)-8-methoxygoniodiol via Co-catalyzed HKR of anti-(2SR, 3RS)-3-methoxy-3-phenyl-1, 2-epoxypropane</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric synthesis of (+)-stagonolide C and (-)-aspinolide A via organocatalysis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient one pot regioselective synthesis of a 3,3 `-spiro-phosphonylpyrazole-oxindole framework via base mediated [1,3]-dipolar cycloaddition reaction of the Bestmann-Ohira reagent with methyleneindolinones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient organocatalytic route for asymmetric total synthesis of stagonolide F</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fluoride-assisted synthesis of 1,4,5,6-tetrahydropyridazines via [4+2] cyclodimerization of in situ-generated azoalkenes followed by a C-N bond cleavage</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of pinolide via L-proline-catalyzed sequential alpha-aminooxylation, horner-wadsworth-emmons olefination and sharpless asymmetric dihydroxylation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient Sn(II)-catalyzed one-pot synthesis of a 3-substituted azetidine-2,4-dione framework</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of key intermediate for (+)-tofacitinib through CoIII(salen)-catalyzed two stereocentered hydrolytic kinetic resolution of (±)-methyl-3-(oxiran-2-yl)butanoate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Two stereocentered HKR of anti-β,β′-diphenylpropanoxirane and anti-3-phenylethyloxiranes catalysed by Co(III)(salen)-OAc complex: enantioselective synthesis of (+)-sertraline and (+)-naproxen</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Iodine-mediated oxidative rearrangement of alpha,beta-unsaturated diaryl ketones: a facile access to 1,2-diaryl diketones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free, radical 1,6-conjugated addition of cyclic ethers with para-quinone methides (p-QMs)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free regioselective cross dehydrogenative coupling of cyclic ethers and aryl carbonyls</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Oxidative Olefination of Benzylamine with an Active Methylene Compound Mediated by Hypervalent Iodine (III)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Visible light mediated, metal and oxidant free highly efficient cross dehydrogenative coupling (CDC) reaction between quinoxalin-2(1H)-ones and ethers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Radical rearrangement of aryl/alkylidene malononitriles via aza michael addition/decynoformylation/addition sequence: an access to alpha-aminonitriles and alpha-aminoamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ti-superoxide catalyzed oxidative amidation of aldehydes with saccharin as nitrogen source: synthesis of primary amides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hypervalent iodine(iii) induced oxidative olefination of benzylamines using Wittig reagents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free, acid-catalyzed 1,6-conjugate addition of NH-sulfoximines to para-quinone methides: accessing to diarylmethine imino sulfanone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Oxidative radical-mediated addition of ethers to quinone imine ketals: an access to hemiaminals</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short enantioselective total synthesis of (+)-tofacitinib</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Visible-light-induced controlled oxidation of N-substituted 1,2,3,4-tetrahydroisoquinolines for the synthesis of 3,4-dihydroisoquinolin-1(2h)-ones and isoquinolin-1(2H)-ones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Acetic acid-catalyzed regioselective C(sp(2))-H bond functionalization of indolizines: concomitant involvement of synthetic and theoretical studies</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hypervalent-iodine-mediated oxidation followed by the acetoxylation/tosylation of alpha-substituted benzylamines to obtain alpha-acyloxy/tosyloxy ketones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Lewis acid triggered N-alkylation of sulfoximines through nucleophilic ring-opening of donor-acceptor cyclopropanes: synthesis of gamma-sulfoximino malonic diesters</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free access to hindered N-alkyl sulfoximines via in-situ generated Aza-oxyallyl cations from functionalized alkyl bromide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Visible light-promoted, photocatalyst-free C(sp(2))-H bond functionalization of indolizines via EDA complexes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (+)-Sedridine, (-)-Allosedridine and their N-Methyl analogs via Maruoka-Keck allylation and CBS reduction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of 3 alkyl and 1,3-Bis(alkyl)indolizine amides from a-bromohydroxamates</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hypervalent-iodine-mediated base-free oxidative olefination of benzylic amines to access α,β-unsaturated ketones</style>