Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Neopentyl alcohol"'
Autor:
Hideo Togo, Masatoshi Ezawa
Publikováno v:
European Journal of Organic Chemistry. 2017:2379-2384
A one-pot protocol to obtain C1-homologated aliphatic nitriles was achieved by treating aromatic and aliphatic aldehydes with the (methoxymethyl)triphenylphosphonium ylide followed by hydrolysis of the resulting methyl vinyl ethers with pTsOH (Ts = p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f676d2dbb6d0d5b474c025533e075041
https://doi.org/10.1002/ejoc.201700277
https://doi.org/10.1002/ejoc.201700277
Akademický článek
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Autor:
A. P. Zeelenberg
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 81:720-728
The slow oxidation of neopentane has been investigated in a static system at 260°. Analysis by means of gas-liquid chromatography (GLC) during the early stages of the combustion showed the presence of isobutene, acetone, isobutyraldehyde, pivalaldeh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::557096832cb0c72843ca39220c45b8de
https://doi.org/10.1002/recl.19620810812
https://doi.org/10.1002/recl.19620810812
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 103:453-461
Primary hydroxy groups as in neopentyl alcohol 7 or neopentylglycol 18 react readily with perfluorobutanesulfonyl fluoride 1 in the presence of 2 equiv. of the nucleophilic 4-dialkylaminopyridines 4 to afford high yields of the corresponding N-alkyl-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e09132efa683b9102dac86c516b3170e
https://doi.org/10.1002/bscb.19941030720
https://doi.org/10.1002/bscb.19941030720
Autor:
Yu Lu, Michael J. Krische
Publikováno v:
Organic Letters. 11:3108-3111
Under the conditions of C-C bond forming transfer hydrogenation, 1,3-propanediol 1 engages in double asymmetric carbonyl allylation to furnish the C(2)-symmetric diol 2. Double ozonolysis of 2 followed by TBS protection delivers aldehyde 3, which is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e88ac892e78e1e3e66f79a070fa6e4c
https://doi.org/10.1021/ol901096d
https://doi.org/10.1021/ol901096d
Publikováno v:
International Journal of Mass Spectrometry. 278:26-31
The dissociation dynamics of energy-selected neopentylamine cations, (CH3)3CCH2NH2+, were studied using threshold photoelectron photoion coincidence (TPEPICO) spectroscopy in which ion time-of-flight (TOF) distributions are recorded as a function of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69758e71ef7c8a40e3f2305735bec9f9
https://doi.org/10.1016/j.ijms.2008.07.036
https://doi.org/10.1016/j.ijms.2008.07.036
Publikováno v:
Journal of Computational Chemistry. 28:1561-1571
The neopentyl and the pinacol rearrangements as examples of Wagner-Meerwein rearrangements were investigated by the use of DFT calculations. As the first reaction, a model of neopentyl chloride (1b) and (H2O)12 was employed. In the reaction, the patt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88738cb9deaa9c8e310685601c070c5a
https://doi.org/10.1002/jcc.20690
https://doi.org/10.1002/jcc.20690
Publikováno v:
Catalysis Communications. 3:25-28
Metal triflates such as Sn(Otf) 2 and La(Otf) 3 act as efficient catalysts for cleaving 2,4,4,-trimethyl-pentane-2-hydroperoxide into neopentyl alcohol and acetone in sulpholane. Compared to H 2 SO 4 , the conventional catalyst for hydroperoxide rear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f14b501e6e08aef84a63164333a2e4e
https://doi.org/10.1016/s1566-7367(01)00071-1
https://doi.org/10.1016/s1566-7367(01)00071-1
Publikováno v:
Journal of computational chemistry. 35(30)
B3LYP calculations were carried out on hydrolysis reactions of monosubstituted(R) phosphate dianion and sulfate monoanion. In the reacting system, water clusters (H2O)22 and (H2O)35 are included to trace reaction paths. For both P and S substrates wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062dace12e29ea3ae0cccf437f49ceaf
https://pubmed.ncbi.nlm.nih.gov/25250540
https://pubmed.ncbi.nlm.nih.gov/25250540
Publikováno v:
Journal of the American Oil Chemists' Society. 78:219-223
Oleic acid (cis-9-octadecenoic acid) was converted in excellent yield to the estolide, which was then esterified with 2,2-dimethypropan-1-ol (neopentyl alcohol), cis-9-octadence-1-ol (oleyl alcohol), and 2-propanol to generate the corresponding estol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94603634de5f3a1dfcd7f6e77db26a32
https://doi.org/10.1007/s11746-001-0248-5
https://doi.org/10.1007/s11746-001-0248-5