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1 een a poorly selective cyclopropanation with ethyl diazoacetate.
2 boxylate complexes and their reactivity with ethyl diazoacetate.
3    The carbene forms by dinitrogen loss from ethyl diazoacetate.
4  also to minimize bimolecular reactions with ethyl diazoacetate.
5 en without slow syringe pump addition of the ethyl diazoacetate.
6 lladium carboxylate dimers, which polymerize ethyl diazoacetate, a carbene precursor in a controlled
7 arbene complex was trapped by reactions with ethyl diazoacetate and (C5H5)Co(PPh3)2 to give cobalt-di
8 alytic variant of the aldol reaction between ethyl diazoacetate and aldehydes is described using a co
9 ium-catalyzed enantioselective aldol between ethyl diazoacetate and aromatic, aliphatic, and alpha,be
10 tioselective catalysts for the conversion of ethyl diazoacetate and terminal acetylenes to chiral cyc
11  and ethers with trimethylsilyldiazomethane, ethyl diazoacetate, and trifluoromethyl-diazomethane hav
12 2-en-1-oyl)oxazolidinones from acetylene and ethyl diazoacetate are described.
13 pha-C-H functionalization in the presence of ethyl diazoacetate as carbene donor (up to 96:4 e.r. and
14 etric catalytic aziridination of imines with ethyl diazoacetate (AZ reaction).
15 scribed starting from an aldehyde, an amine, ethyl diazoacetate, B(OPh)(3), and a molecule of a vault
16 romocyclopropanes 21 and 22 by reaction with ethyl diazoacetate catalyzed by Rh2(OAc)4 were futile.
17 e enzymatic cyclopropanation of allenes with ethyl diazoacetate (EDA) catalyzed by an iridium-contain
18 yl boranes, the reaction of borane (BH3) and ethyl diazoacetate (EDA) generates dimer, trimer, and ol
19 o a dilute solution of diazomethane (DM) and ethyl diazoacetate (EDA) in ether at 0 degrees C.
20  asymmetric cyclopropanation of alkenes with ethyl diazoacetate (EDA).
21 side chains undergo covalent modification by ethyl diazoacetate (EDA).
22 r selective cyclopropanation of alkenes with ethyl diazoacetate (EDA).
23 metric cyclopropanation of vinyl esters with ethyl diazoacetate (EDA).
24 itial DBU-promoted "aldol" condensation with ethyl diazoacetate followed by in situ oxidation with IB
25             Addition of carbene derived from ethyl diazoacetate gave cyclopropane 15 as the major pro
26  copper or rhodium salts, in the presence of ethyl diazoacetate, giving ethyl cis-N-methyl-3-ethenyl
27 catalysts for cyclopropanation of olefins by ethyl diazoacetate, giving excellent yields (66-94%).
28 y of the reactions of carbonyl compounds and ethyl diazoacetate in the presence of a Bronsted acid ca
29 uted allyl sulfides (2a-i) were reacted with ethyl diazoacetate in the presence of copper triflate (C
30 e olefination of a variety of aldehydes with ethyl diazoacetate in the presence of triphenylphosphine
31 rmediates from the 270 nm photoexcitation of ethyl diazoacetate in various solvents and the changes i
32 inuclear Mg-catalyzed asymmetric addition of ethyl diazoacetate into several aldehydes, oxidation of
33 atalytic aziridination of N-aryl imines with ethyl diazoacetate is also described.
34 f N-dianisylmethylimines (N-DAM-imines) with ethyl diazoacetate is developed with chiral catalysts pr
35 sites of hexane or pentane, whereas acceptor ethyl diazoacetate leads to an unprecedented level of pr
36 d and finally the reaction of the imine with ethyl diazoacetate mediated by the imino-BOROX catalyst
37 nt reactions of carbonyl ylides derived from ethyl diazoacetate or alpha-aryl-alpha-diazoesters.
38 f the soluble polymer-bound catalyst and the ethyl diazoacetate reactant.
39                       The reaction of 1 with ethyl diazoacetate resulted in a tin-substituted ketene
40 kenes are cyclopropanated in the presence of ethyl diazoacetate to give CHF(2) -containing cyclopropa
41  the reaction between aromatic aldehydes and ethyl diazoacetate to produce 3-hydroxy-2-arylacrylic ac
42 he rhodium-catalyzed reaction of Ph(2)S with ethyl diazoacetate) to N-acylhydrazones promoted by a ch
43 d through addition of terminal ynamides with ethyl diazoacetate under copper catalysis for the first
44                        Cyclopropanation with ethyl diazoacetate was concluded to involve an earlier t
45 ion of 4-allyl-1,2-dimethoxybenzene (4) with ethyl diazoacetate, which after bromination with Br2 gav
46 ult is a sharp contrast to the reaction with ethyl diazoacetate, which results in cyclopropanation of
47  to results from intermolecular reactions of ethyl diazoacetate with allyl ethyl ether, intermolecula
48                Rhodium-catalyzed reaction of ethyl diazoacetate with methylenecyclopropane 19, obtain