Keywords: N-یدوزوکسی سیمید; Azulene; Orexin receptor; Potentiator; Agonist; Antagonist; Sleep-wake regulation; BINAP; 2,2â²-bis(diphenylphosphino)-1,1â²-binaphthyl; CHO; Chinese hamster ovary (cells); dppf; 1,1â²-bis(diphenylphosphino)ferrocene; EDC; 1-ethyl-3-(3-dimethylaminopro
مقالات ISI N-یدوزوکسی سیمید (ترجمه نشده)
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Regioselective 1,2-additions of alcohols to allenamides mediated by N-Iodosuccinimide: Synthesis of N,O-aminals
Keywords: N-یدوزوکسی سیمید; Allenamides; Alcohols; N,O-aminals; N-Iodosuccinimide; Regioselective;
Synthesis and evaluation of analogs of 5â²-(((Z)-4-amino-2-butenyl)methylamino)-5â²-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity
Keywords: N-یدوزوکسی سیمید; AdoMet; S-adenosyl-l-methionine; AdoMetDC; S-adenosylmethionine decarboxylase; BBB; bloodbrain barrier; Boc; tert-butoxycarbonyl; BSA; N,O-bis(trimethylsilyl)acetamide; CNS; central nervous system; DEAD; diethyl azodicarboxylate; DIAD; diisopropyl azodica
Structure-based design and synthesis of imidazo[1,2-a]pyridine derivatives as novel and potent Nek2 inhibitors with in vitro and in vivo antitumor activities
Keywords: N-یدوزوکسی سیمید; Nek2 inhibitors; Imidazo[1,2-a]pyridine; Antitumor activity; Selectivity; Nek2; NIMA-related kinase 2; Nlp; ninein-like protein; SAC; spindle assembly checkpoint; Mad1/2; mitotic arrest deficient 1/2; Hec1; highly expressed in cancer 1; CIN; chromosome in
An intermolecular iodoamination of allenamides with sulfonamides mediated by N-iodosuccinimide
Keywords: N-یدوزوکسی سیمید; Iodoamination; Allenamides; Sulfonamides; N-Iodosuccinimide; Iodine-substituted allylamino Z-enamides;
A concise approach for the synthesis of 3-iodoindoles and 3-iodobenzo[b]furans via Ph3P-catalyzed iodocyclization
Keywords: N-یدوزوکسی سیمید; 3-Iodoindoles; 3-Iodobenzo[b]furans; Triphenylphosphine; Iodocyclization; N-iodosuccinimide;
Intramolecular aminochalcogenation and diamination of alkenes employing N-iodosuccinimide
Keywords: N-یدوزوکسی سیمید; Aminosulfuration; Diamination; Alkenes; N-Iodosuccinimide; Aminooxygenation;
Synthesis of cellulose triacetate from cotton cellulose by using NIS as a catalyst under mild reaction conditions
Keywords: N-یدوزوکسی سیمید; N-Iodosuccinimide; Cellulose triacetate; Acetylation; Cotton cellulose; Raman;
Synthesis and biological evaluation of pyridinone analogues as novel potent HIV-1 NNRTIs
Keywords: N-یدوزوکسی سیمید; HIV; human immunodeficiency virus; NNRTIs; non-nucleoside reverse transcriptase inhibitors; SARs; structure and activity relationships; HAART; highly active antiretroviral therapy; RT; reverse transcriptase; NVP; nevirapine; DLV; delavirdine; EFV; efavire
Stereoselective synthesis of 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors
Keywords: N-یدوزوکسی سیمید; HMG-CoA reductase inhibitors; Statins; Chiral β-hydroxy-δ-lactone; Chiral 3,5-syn-diol acid; Asymmetric synthesis; Ac; acetyl; Ar; aryl; Bn; benzyl; Bz; benzoyl; n-Bu; butyl; t-Bu; tert-butyl; CDI; 1,1â²-carbonyldiimidazole; BINOL; 1,1â²-bi-2-naphthol
Novel synthesis of carbohydrate fused α-amino γ-lactams and glycopeptides by NIS mediated ring opening of donor–acceptor substituted cyclopropanes
Keywords: N-یدوزوکسی سیمید; Donor–acceptor cyclopropane; Ring opening; γ-Lactam; Glycopeptide; N-Iodosuccinimide; Reductive cyclization
Metal-free synthesis of 1H-indole-2-carbaldehydes by N-iodosuccinimide-mediated cyclization of 1-(2â²-anilinyl)prop-2-yn-1-ols in water. A formal synthesis of (R)-calindol
Keywords: N-یدوزوکسی سیمید; Cycloisomerization; N-Iodosuccinimide; 1H-Indole-2-carbaldehydes; Propargylic alcohols; Water;
Metal-free N-iodosuccinimide-catalyzed mild oxidative C-H bond amination of benzoxazoles
Keywords: N-یدوزوکسی سیمید; Green chemistry; Oxidative amination; C-H activation; Homogeneous catalysis; N-Iodosuccinimide;
NBS or DEAD as effective reagents in α-thiocyanation of enolizable ketones with ammonium thiocyanate
Keywords: N-یدوزوکسی سیمید; DEAD; diethyl azodicarboxylate; NBS; N-bromosuccinimide; NCS; N-chlorosuccinimide; NIS; N-iodosuccinimide; NTS; N-thiocyanatosuccinimide; Ketones; N-Bromosccinimide; Ammonium thiocyanate; α-Ketothiocyanates;
N-Iodosuccinimide (NIS) a novel and effective catalyst for the cyanosilylation of aldehydes under mild reaction conditions
Keywords: N-یدوزوکسی سیمید; Cyanosilylation; Aldehydes; N-Iodosuccinimide; Cyanohydrins
Enantioselective synthesis of steroids
Keywords: N-یدوزوکسی سیمید; Steroids; Asymmetric inductions; Pool chiral; Enantioselectivity; Resolution; acac; acetylacetonate; 9-BBN; 9-bora-bicyclo[3.3.1]nonane; BHT; 2,6-di-tert-butyl-4-methylphenol; BINAP; 2,2â²-bis(diphenylphosphino)-1,1â²-binaphthyl; Binol; 1,1â²-binaphtha
Synthetic applications of fluorous solid-phase extraction (F-SPE)
Keywords: N-یدوزوکسی سیمید; Fluorous; Light fluorous; Fluorous silica gel; Fluorous solid-phase extraction (F-SPE); Reverse F-SPE; Plate-to-plate SPE; Parallel synthesis; High-throughput synthesis; Solution-phase synthesis; Separation; Reagents; Reactants; Catalysts; Chiral auxiliar
Synthesis and role of glycosylthio heterocycles in carbohydrate chemistry
Keywords: N-یدوزوکسی سیمید; Thioglycoside; Glycosidation reaction; Glycosylating agents; Heterocycles; O-Glycosides; C-Glycosidation; Leaving groups; Anomeric centers; SPy; thiopyridyl; SQu; thioquinolinyl; SIm; thioimdazolyl; STh; thiothiazolyl; SBth; thiobenzothiazolyl; SBox; thio
Naphtho[2,3-c]furan-4,9-diones and related compounds: theoretically interesting and bioactive natural and synthetic products
Keywords: N-یدوزوکسی سیمید; Naphtho[2,3-c]furan-4,9-diones; Naphtho[2,3-c]furan-4(9H)-ones; Naphtho[2,3-c]furan; Isofuranonaphthoquinones; Ac; acetyl; AIBN; 2â²-azobis(isobutyronitrile); Ar; aryl; Bn; benzyl; BOM; benzyloxymethyl; But; tert-butyl; CSA; camphor-10-sulfonic acid; DBU
Use of O-glycosylation in total synthesis
Keywords: N-یدوزوکسی سیمید; O-Glycosylation; Total synthesis; Ac; acetyl; ACF; activated carbon fiber; AIBN; 2,2â²-azobiisobutyronitrile; Alloc; allyloxycarbonyl; Ar; aryl; AtOH; 7-aza-1-hydroxy-1H-benzotriazole; BF3(Et2O); boron trifluoride etherate; DMB; 3,4-dimethoxybenzyl; DMTS