ライフサイエンスコーパス: ethereal

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1 Diisoamyl sulfide has a mild, ethereal, agreeable aroma, its synthesis is economical a

2 Lithium hexamethyldisilazide complexes with ethereal and ester donor ligands (THF, diethyl ether, MT

3 s reaction is applicable to breaking the key ethereal bond found in lignin-related polymers.

4 keleton and contain a strained five-membered ethereal bridge, structural features that have proven ch

5 o 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction.

6 Nelson describes 'stress' as a 'notoriously ethereal concept'.

7 Dependencies on THF and other ethereal cosolvents suggest that secondary-shell solvati

8 By passing ethereal diazomethane over peptides on strong cation exc

9 conjugation among the aromatic rings and the ethereal groups.

10 r C-H bond types (i.e., allylic > benzylic > ethereal > 3 degrees > 2 degrees >> 1 degrees ).

11 converted to the halo ketone with anhydrous ethereal hydrogen halide.

12 Our work suggests that steric hindrance of ethereal ligands plays an important role in the aggregat

13 ation only, microsolvation with coordinating ethereal ligands, and a combination of the microsolvatio

14 lack of steric effects from the coordinating ethereal ligands.

15 HF but as a disolvated dimer in monodentate, ethereal, non-THF solvents, whereas (E)-1 was always mon

16 The H-bonding between silanol and ethereal O perturbs the band positions attributed to vib

17 s of fruit flies, suggests that even in this ethereal realm these creatures have much to contribute.

18 ach is mediated by a room-temperature stable ethereal solution of a difluoroallene indium intermediat

19 tegy that exposes glycerophospholipids to an ethereal solution of diazomethane and acid, derivatizing

20 Addition of BF(3).OEt(2) to ethereal solutions of the Ni(II) beta-diketiminates [Me(

21 of the triamine-solvated monomers with their ethereal-solvated dimer counterparts was probed by using

22 Thus, the identity and concentration of an ethereal solvent can dramatically affect configurational

23 d Ru-Macho-BH (1) at 125-165 degrees C in an ethereal solvent has been developed (initial turnover fr

24 opropyl ether by flash photolysis of DTBP in ethereal solvent react with TPZ more slowly than do kety

25 s involve preformed Grignard reagents in dry ethereal solvent that typically react, e.g., with aryl h

26 ied amide/nBuLi mixed aggregates in both the ethereal solvent THF (1:1 dimer) and the hydrocarbon sol

27 in 18 examples using 5 mol % B(C6F5)3 in an ethereal solvent.

28 tailed picture of the solution structures in ethereal solvents (usually in mixtures of THF and dimeth

29 ies were observed for reactions conducted in ethereal solvents and at lower temperatures between N-pr

30 ,N-dimethyl 4-fluorophenylacetamide (3-H) in ethereal solvents and in the presence of cosolvent addit

31 des proceeded in the absence of coordinating ethereal solvents at ambient temperature without the add

32 mines can be deprotonated in the presence of ethereal solvents exclusively at the cis-vinylic positio

33 s were performed to determine the effects of ethereal solvents on the aggregation state of lithium di

34 Solvation in ethereal solvents was modeled by a combination of specif

35 donor denticity, i.e. ligand strength of the ethereal solvents which act as ligands to form solvated

36 raalkylcuprates are not fully dissociated in ethereal solvents, but partly form Li(+)Me(3)CuR(-) cont

37 ng coordination chemistry of Mg(BH(4))(2) in ethereal solvents.

38 2) and MgBr(2) is viable in the coordinating ethereal solvents.

39 odels for ion pair displacement reactions in ethereal solvents.

40 monomers, dimers, and trimers in a number of ethereal solvents.

41 thiodiamines and the effects of solvation by ethereal solvents.

42 LDA and LiTMP to form mixed cyclic dimers in ethereal solvents.

43 re, but the resulting dianion is quenched by ethereal solvents.

44 gth of the adsorbate and the position of the ethereal unit along the hydrocarbon chain.

45 nvited Morton to demonstrate the use of his "ethereal vapor" for anesthesia in a minor operation on O

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