Nondissociative chain walking as a strategy in catalytic organic synthesis
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.07.029
Alkylation reactions of benzothiazoles with N,N-dimethylamides catalyzed by the two-component system under visible light
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.064
Alstobrogaline, an unusual pentacyclic monoterpenoid indole alkaloid with aldimine and aldimine-N-oxide moieties from Alstonia scholaris
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.02.018
Ultraviolet irradiation of terarylenes: A facile, efficient, and environmentally friendly method for the synthesis of fused polycyclic products
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.063
Eosin Y catalysed visible-light mediated aerobic oxidation of tertiary amines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151041
A new strategy for utilizing activated CH-group to construct a FRET platform for ratiometric sensing of cyanides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.010
Ca(II)-catalyzed diastereoselective formal [4+2] annulation of a 3-component solvent-free povarov reaction
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.021
α-Amidoboronate esters by amide-directed alkane C H borylation
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.020
An efficient synthesis of 2-isoxazolines from α-haloketone oximes and dimethyl sulfonium salts
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.062
Chiral Brønsted acid-catalyzed Friedel–Crafts reaction of 3-indolylsulfamidates with indoles: Synthesis of enantioenriched bisindolylmethane sulfamates
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.003
Colorimetric and ratiometric sensors derivated from natural building blocks for fluoride ion detection
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151330
PhI(OAc)2-mediated alkoxyoxygenation of β,γ-unsaturated ketoximes: Preparation of isoxazolines bearing two contiguous tetrasubstituted carbons
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.046
Heterogeneous gold-catalyzed oxidative cross-coupling of propargylic acetates with arylboronic acids leading to (E)-α-arylenones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.11.053
[4 + 3]-Cycloaddition of aza-o-quinone methides and azomethine imines to make 1,2,4-triazepines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.038
First Cp*Co(III)-Catalyzed Mizoroki-Heck Coupling Reactions of Alkenes and Aryl bromide/Iodide
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151283
Unexpected photochemical transformation of imidazole derivatives containing the 5-hydroxy-2-methyl-4H-pyran-4-one moiety. Environmentally friendly method for the synthesis of substituted imidazo[1,5-a]pyridine-5,8-diones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151080
Copper-catalyzed enantioselective addition of alcohols to isatin-derived ketimines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.03.049
Thalicfoetine, a novel isoquinoline alkaloid with antibacterial activity from Thalictrum foetidum
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151135
Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.04.014
First synthesis and further derivatization of furo[3,2-c]pyrazol-6-ones
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.01.021
Simple one pot synthesis of ketone from carboxylic acid using DCC as an activator
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.04.030
Unexpected intramolecular nucleophilic cyclization of ureidoacetamide: A novel route towards the synthesis of 2,4,5-trisubsituted oxazoles
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.028
Iron-catalyzed δ-selective conjugate addition of methyl and cyclopropyl Grignard reagents to α,β,γ,δ-unsaturated esters and amides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.043
Investigation of α-amino acid N-carboxyanhydrides by X-ray diffraction for controlled ring-opening polymerization
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.028
Three-component couplings for the synthesis of pyrroloquinoxalinones by azomethine ylide 1,3-dipolar cycloaddition chemistry
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151023
Enantioselective synthesis of chiral carbocyclic pyrimidine nucleosides via asymmetric cyclopropanation
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151183
Epoxide as precatalyst for metal-free catalytic transesterification
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.056
Violet/deep-blue fluorescent organic light-emitting diode based on high-efficiency novel carbazole derivative with large torsion angle
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151340
Total synthesis of the tricyclic humulanolide wilfolide B
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.058
I2/TBHP mediated multiple C H bonds functionalization of azaarenes with methylarenes to synthesize iodoisoquinolinones via iodination/N-benzylation/amidation sequence
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151328
Propargyl α-aryl-α-diazoacetates as robust reagents for the effective C-H bond functionalization of 1,3-diketones via scandium catalysis
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.026
First total synthesis of versicotide D and analogs
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151281
Triphenylene based metal-pyridine cages
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151202
Facile and practical synthesis of π-extended oxepins by benzannulation and intramolecular cyclization
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.008
Type-II Pauson-Khand reaction of 1,8-enyne in the attempt of building 7/5 ring of (-)-caribenol A and DFT understanding
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151001
Functionalization of silica gel by ultrasound-assisted surface Suzuki coupling
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.07.028
The DFT study on Rh–C bond dissociation enthalpies of (iminoacyl)rhodium(III)hydride and (iminoacyl)rhodium(III)alkyl
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.042
Xanthate-mediated synthesis of functional bis(γ-thiolactones)
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.004
First asymmetric enantioselective total synthesis of phenanthridine alkaloid, (S)-(+)-asiaticumine and its enantiomer
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151278
Total synthesis and determination of the absolute configuration of paralemnolin C and biological studies of eremophilane derivatives
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.05.026
Triptycene-scaffolded tetraphenylethylenes with irregular temperature-dependence AIE
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2018.12.069
Synergic effect of hydrogen bonding and dipole repulsion in the ring-closing metathesis of N-homoallyl-2-(hydroxymethyl)acrylamides
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.011
Room Temperature Pd(0)/Ad3P-Catalyzed Coupling Reactions of Aryl Chlorides with Bis(pinacolato)diboron
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.01.042
Diphosphination of ortho-quinone methide precursors with diphosphines
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.06.055
Photoaddition reactions of azomethine ylides generated from α-aminonitriles to fullerene C60: Formation of fulleropyrrolidines and reaction efficiencies changes depending on reaction conditions
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151208
Transfer hydrogenation of ketones catalyzed by 2,6‐bis(triazinyl)pyridine ruthenium complexes: The influence of alkyl arms
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.150993
Studies towards the stereoselective total synthesis of Gliomasolide A
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151169
One-pot synthesis of new iso-DPP derivatives from terminal alkynes and isocyanates
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.151079
Stereoconvergent synthesis of N-Boc-(2R,3S)-3-hydroxy-2-phenylpiperidine
来源期刊:Tetrahedron LettersDOI:10.1016/J.TETLET.2019.02.005
Alkaloids of NIRAM, natural dye from Polygonum tinctorium, and their anti-inflammatory activities
来源期刊:Tetrahedron LettersDOI:10.1016/j.tetlet.2019.151130