ライフサイエンスコーパス: ethyl diazoacetate

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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 arbene complex was trapped by reactions with ethyl diazoacetate and (C5H5)Co(PPh3)2 to give cobalt-di

7 ium-catalyzed enantioselective aldol between ethyl diazoacetate and aromatic, aliphatic, and alpha,be

8 tioselective catalysts for the conversion of ethyl diazoacetate and terminal acetylenes to chiral cyc

9 2-en-1-oyl)oxazolidinones from acetylene and ethyl diazoacetate are described.

10 etric catalytic aziridination of imines with ethyl diazoacetate (AZ reaction).

11 scribed starting from an aldehyde, an amine, ethyl diazoacetate, B(OPh)(3), and a molecule of a vault

12 romocyclopropanes 21 and 22 by reaction with ethyl diazoacetate catalyzed by Rh2(OAc)4 were futile.

13 yl boranes, the reaction of borane (BH3) and ethyl diazoacetate (EDA) generates dimer, trimer, and ol

14 o a dilute solution of diazomethane (DM) and ethyl diazoacetate (EDA) in ether at 0 degrees C.

15 side chains undergo covalent modification by ethyl diazoacetate (EDA).

16 asymmetric cyclopropanation of alkenes with ethyl diazoacetate (EDA).

17 r selective cyclopropanation of alkenes with ethyl diazoacetate (EDA).

18 itial DBU-promoted "aldol" condensation with ethyl diazoacetate followed by in situ oxidation with IB

19 Addition of carbene derived from ethyl diazoacetate gave cyclopropane 15 as the major pro

20 copper or rhodium salts, in the presence of ethyl diazoacetate, giving ethyl cis-N-methyl-3-ethenyl

21 catalysts for cyclopropanation of olefins by ethyl diazoacetate, giving excellent yields (66-94%).

22 uted allyl sulfides (2a-i) were reacted with ethyl diazoacetate in the presence of copper triflate (C

23 e olefination of a variety of aldehydes with ethyl diazoacetate in the presence of triphenylphosphine

24 inuclear Mg-catalyzed asymmetric addition of ethyl diazoacetate into several aldehydes, oxidation of

25 atalytic aziridination of N-aryl imines with ethyl diazoacetate is also described.

26 f N-dianisylmethylimines (N-DAM-imines) with ethyl diazoacetate is developed with chiral catalysts pr

27 d and finally the reaction of the imine with ethyl diazoacetate mediated by the imino-BOROX catalyst

28 nt reactions of carbonyl ylides derived from ethyl diazoacetate or alpha-aryl-alpha-diazoesters.

29 f the soluble polymer-bound catalyst and the ethyl diazoacetate reactant.

30 The reaction of 1 with ethyl diazoacetate resulted in a tin-substituted ketene

31 the reaction between aromatic aldehydes and ethyl diazoacetate to produce 3-hydroxy-2-arylacrylic ac

32 he rhodium-catalyzed reaction of Ph(2)S with ethyl diazoacetate) to N-acylhydrazones promoted by a ch

33 Cyclopropanation with ethyl diazoacetate was concluded to involve an earlier t

34 ion of 4-allyl-1,2-dimethoxybenzene (4) with ethyl diazoacetate, which after bromination with Br2 gav

35 to results from intermolecular reactions of ethyl diazoacetate with allyl ethyl ether, intermolecula

36 Rhodium-catalyzed reaction of ethyl diazoacetate with methylenecyclopropane 19, obtain

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