Iron(II) complexes bearing tridentate PNP pincer-type ligands as catalysts for the selective formation of 3-hydroxyacrylates from aromatic aldehydes and ethyl diazoacetate
10.1021/om060802o · doi-reference
Iron Lewis acid catalyzed reactions of aromatic aldehydes with ethyl diazoacetate: unprecedented formation of 3-hydroxy-2-arylacrylic acid ethyl esters by a unique 1,2-aryl shift
10.1021/jo972142q · doi-reference
Iron Lewis acid catalyzed reactions of phenyldiazomethane with aromatic aldehydes
10.1016/s0040-4020(97)10287-3 · doi-reference
Synthesis of asymmetric iron–pybox complexes and their application to aziridine forming reactions
10.1016/j.tetlet.2004.10.047 · doi-reference
An explanation for the apparent cis-aziridine selectivity in the iron Lewis acid-catalyzed reaction of N-benzylidene aniline and ethyl diazoacetate
10.1016/s0022-328x(01)00886-5 · doi-reference
Catalytic preparation of aziridines with an iron Lewis acid
10.1021/jo9804792 · doi-reference
Novel multicomponent reactions via trapping of protic onium ylides with electrophiles
10.1021/ar300340k · doi-reference
Iron porphyrin-catalyzed three-component reaction of ethyl diazoacetate with aliphatic amines and β,γ-unsaturated α-keto esters
10.1021/ol403011r · doi-reference
Iron-catalyzed synthesis of glycine derivatives via carbon–nitrogen bond cleavage using diazoacetate
10.1039/c0cc03781h · doi-reference
Iron porphyrin-catalyzed olefination of ketenes with diazoacetate for the enantioselective synthesis of allenes
10.1021/ja068642v · doi-reference
A newly-designed PE-supported arsine for efficient and practical catalytic Wittig olefination
10.1039/c1cc16747b · doi-reference
Efficient and stereoselective synthesis of β-trifluoromethyl α,β-unsaturated esters via iron(III) porphyrin-catalyzed olefination of Ketones
10.1021/jo034509z · doi-reference
Iron porphyrin-catalyzed olefination of carbonyl compounds with ethyl diazoacetate
10.1021/om020904o · doi-reference
Acid-promoted olefination of ketones by an iron(III) porphyrin complex
10.1021/ol0347444 · doi-reference
Generation of phosphoranes derived from phosphites. A new class of phosphorus ylides leading to high E selectivity with semi-stabilizing groups in Wittig olefinations
10.1021/ja029573x · doi-reference
An efficient method for the olefination of aldehydes with ethyl diazoacetate using iron(II) phthalocyanine as catalyst
10.1007/s10562-004-7929-1 · doi-reference
Efficient aldehyde olefination reactions catalyzed by an iron porphyrin complex in an ionic liquid
10.1016/j.tetlet.2004.08.070 · doi-reference
Iron(III) and ruthenium(II) porphyrin complex-catalyzed selective olefination of aldehydes with ethyl diazoacetate
10.1021/jo0341158 · doi-reference
Update: an efficient synthesis of poly(ethylene glycol)-supported iron(II) porphyrin using a click reaction and its application for the catalytic olefination of aldehydes
10.1002/adsc.201100289 · doi-reference
A new and efficient method for the selective olefination of aldehydes with ethyl diazoacetate catalyzed by an iron(II) porphyrin complex
10.1021/ja016721v · doi-reference
Iron-catalyzed reaction of propargyl sulfides and trimethylsilyldiazomethane
10.1021/jo010247u · doi-reference
Iron-catalyzed Doyle–Kirmse reaction of allyl sulfides with (trimethylsilyl)diazomethane
10.1021/ol005740r · doi-reference
Rearrangements of ylides generated from reactions of diazo compounds with allyl acetals and thioketals by catalytic methods. Heteroatom acceleration of the [2,3]-sigmatropic rearrangement
10.1021/jo00185a014 · doi-reference
Reaktionen des diazomethans mit diallylsulfid und allyläthern unter kupfersalz-katalyse
10.1002/cber.19681010333 · doi-reference
Catalytic asymmetric reaction with water: enantioselective synthesis of α-hydroxyesters by copper-carbenoid O–H insertion reaction
10.1002/anie.200704651 · doi-reference
Catalytic enantioselective O–H insertion reactions
10.1021/ja0607739 · doi-reference
Enantioselective transition-metal-catalyzed heteroatom-hydrogen bonds insertion reactions
10.1021/ar300051u · doi-reference
Enantioselective iron-catalysed O–H bond insertions
10.1038/nchem.651 · doi-reference
Regioselectivity in Lewis acids catalyzed X–H (O, S, N) insertions of methyl styryldiazoacetate with benzyl alcohol, benzyl thiol, and aniline
10.1016/j.tetlet.2007.04.046 · doi-reference
Indium triflate: a mild and efficient Lewis acid catalyst for O–H insertion reactions of α-diazo ketones
10.1016/s0040-4039(02)00489-6 · doi-reference
Catalytic activation of diazo compounds using electron-rich, defined iron complexes for carbene-transfer reactions
10.1002/anie.201201409 · doi-reference
Cytochrome P450-catalyzed insertion of carbenoids into N–H bonds
10.1039/c3sc52535j · doi-reference
O–H insertion and tandem N–H insertion/cyclization reactions using an iron porphyrin as catalyst with diazo compounds as carbene sources
10.1142/s1088424610001982 · doi-reference
Iron(III) corroles and porphyrins as superior catalysts for the reactions of diazoacetates with nitrogen- or sulfur-containing nucleophilic substrates: synthetic uses and mechanistic insights
10.1002/chem.200701885 · doi-reference
Iron porphyrin catalyzed N–H insertion reactions with ethyl diazoacetate
10.1021/om0610997 · doi-reference
Iron-catalyzed C–H functionalization of indoles
10.1002/adsc.201100334 · doi-reference
Rhodium-catalyzed [3 + 2] annulation of indoles
10.1021/ja9078094 · doi-reference
Catalytic C–H insertions using iron(III) porphyrin complexes
10.1021/om7007502 · doi-reference
Catalytic carbene insertion into C–H bonds
10.1021/cr900239n · doi-reference
Transition metal-catalyzed C–H activation reactions: diastereoselectivity and enantioselectivity
10.1039/b816707a · doi-reference
