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1                Diisoamyl sulfide has a mild, ethereal, agreeable aroma, its synthesis is economical a
2 g sites such as secondary alpha-amino, alpha-ethereal, allyl, and vinyl sites, providing great versat
3 d ((Em)L)H and intermolecular insertion into ethereal and allylic C-H bonds.
4 severely understudied in comparison to their ethereal and amino counterparts.
5  Lithium hexamethyldisilazide complexes with ethereal and ester donor ligands (THF, diethyl ether, MT
6 asic amines and competing sites for allylic, ethereal, and benzylic amination.
7 der participants considered the mind as more ethereal, as more resilient to the obliteration of one's
8 s reaction is applicable to breaking the key ethereal bond found in lignin-related polymers.
9 keleton and contain a strained five-membered ethereal bridge, structural features that have proven ch
10 o 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction.
11 ubstrates contain up to eight discrete alpha-ethereal C-H bonds, we observed site-selectivity in each
12  Nelson describes 'stress' as a 'notoriously ethereal concept'.
13                Dependencies on THF and other ethereal cosolvents suggest that secondary-shell solvati
14                                   By passing ethereal diazomethane over peptides on strong cation exc
15 e Dualists-they tend to perceive the mind as ethereal, distinct from the body.
16 r intuitive dualism, however, the mind seems ethereal, distinct from the body.
17 e Dualists-they tacitly consider the mind as ethereal, distinct from the body.
18 conjugation among the aromatic rings and the ethereal groups.
19 r C-H bond types (i.e., allylic > benzylic > ethereal > 3 degrees > 2 degrees >> 1 degrees ).
20  as is the question of why only select alpha-ethereal hydrogen atoms are targeted in the reaction.
21  converted to the halo ketone with anhydrous ethereal hydrogen halide.
22                    Switching from diamine to ethereal ligands inverts the sense of asymmetric inducti
23   Our work suggests that steric hindrance of ethereal ligands plays an important role in the aggregat
24 ation only, microsolvation with coordinating ethereal ligands, and a combination of the microsolvatio
25 lack of steric effects from the coordinating ethereal ligands.
26 bling it to establish three H-bonds with the ethereal macrocycle.
27 , the self is aligned more strongly with the ethereal mind, rather than with the body.
28 HF but as a disolvated dimer in monodentate, ethereal, non-THF solvents, whereas (E)-1 was always mon
29            The H-bonding between silanol and ethereal O perturbs the band positions attributed to vib
30 d to establish three hydrogen bonds with the ethereal oxygens of the macrocycle.
31 s of fruit flies, suggests that even in this ethereal realm these creatures have much to contribute.
32 ach is mediated by a room-temperature stable ethereal solution of a difluoroallene indium intermediat
33 tegy that exposes glycerophospholipids to an ethereal solution of diazomethane and acid, derivatizing
34                  Addition of BF(3).OEt(2) to ethereal solutions of the Ni(II) beta-diketiminates [Me(
35 of the triamine-solvated monomers with their ethereal-solvated dimer counterparts was probed by using
36   Thus, the identity and concentration of an ethereal solvent can dramatically affect configurational
37 d Ru-Macho-BH (1) at 125-165 degrees C in an ethereal solvent has been developed (initial turnover fr
38 opropyl ether by flash photolysis of DTBP in ethereal solvent react with TPZ more slowly than do kety
39 s involve preformed Grignard reagents in dry ethereal solvent that typically react, e.g., with aryl h
40 ied amide/nBuLi mixed aggregates in both the ethereal solvent THF (1:1 dimer) and the hydrocarbon sol
41  in 18 examples using 5 mol % B(C6F5)3 in an ethereal solvent.
42 tailed picture of the solution structures in ethereal solvents (usually in mixtures of THF and dimeth
43 ies were observed for reactions conducted in ethereal solvents and at lower temperatures between N-pr
44 ,N-dimethyl 4-fluorophenylacetamide (3-H) in ethereal solvents and in the presence of cosolvent addit
45 des proceeded in the absence of coordinating ethereal solvents at ambient temperature without the add
46                          Dipolar aprotic and ethereal solvents comprise just over 40% of all organic
47 mines can be deprotonated in the presence of ethereal solvents exclusively at the cis-vinylic positio
48 tion of ethers mediated by N-chloroimides in ethereal solvents in the presence of lithium tert-butoxi
49 the ubiquitous nature of dipolar aprotic and ethereal solvents is discussed with respect to the physi
50 ng imposed on the use of dipolar aprotic and ethereal solvents is discussed.
51 s were performed to determine the effects of ethereal solvents on the aggregation state of lithium di
52 ful organic peroxides (OPs) generated in old ethereal solvents via auto-oxidation.
53                                 Solvation in ethereal solvents was modeled by a combination of specif
54 donor denticity, i.e. ligand strength of the ethereal solvents which act as ligands to form solvated
55 raalkylcuprates are not fully dissociated in ethereal solvents, but partly form Li(+)Me(3)CuR(-) cont
56      In the presence of NaNH(2) or n-BuLi in ethereal solvents, dialkyl sulfones react with styrenes
57 ng coordination chemistry of Mg(BH(4))(2) in ethereal solvents.
58 2) and MgBr(2) is viable in the coordinating ethereal solvents.
59 odels for ion pair displacement reactions in ethereal solvents.
60 monomers, dimers, and trimers in a number of ethereal solvents.
61 thiodiamines and the effects of solvation by ethereal solvents.
62 d reaction conditions using weakly donating, ethereal solvents.
63 LDA and LiTMP to form mixed cyclic dimers in ethereal solvents.
64 re, but the resulting dianion is quenched by ethereal solvents.
65 ve detection of hazardous OPs present in old ethereal solvents.
66 gth of the adsorbate and the position of the ethereal unit along the hydrocarbon chain.
67 nvited Morton to demonstrate the use of his "ethereal vapor" for anesthesia in a minor operation on O
68 erved for electron-rich C-H bonds (tertiary, ethereal), while greater catalyst loadings or elevated r