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Quoted phrases not found in phrase index: "(3Z)-3-hexene", "cis-g-hexylene", "cis-hexene-3"
Page 1
Natural tetraponerines: a general synthesis and antiproliferative activity.
Bosque I, Gonzalez-Gomez JC, Loza MI, Brea J. Bosque I, et al. J Org Chem. 2014 May 2;79(9):3982-91. doi: 10.1021/jo500446f. Epub 2014 Apr 14. J Org Chem. 2014. PMID: 24731136 Free article.
A cross-metathesis reaction of the second aminoallylation product with cis-3-hexene is used to elongate the side chain up to 5 carbons so as to prepare the tetraponerines T5 to T8. ...
A cross-metathesis reaction of the second aminoallylation product with cis-3-hexene is used to elongate the side chain …
Rate coefficients for the reaction of OH radicals with cis-3-hexene: an experimental and theoretical study.
Barbosa Tda S, Peirone S, Barrera JA, Abrate JP, Lane SI, Arbilla G, Bauerfeldt GF. Barbosa Tda S, et al. Phys Chem Chem Phys. 2015 Apr 14;17(14):8714-22. doi: 10.1039/c4cp05760k. Epub 2015 Mar 4. Phys Chem Chem Phys. 2015. PMID: 25738192
The kinetics of the cis-3-hexene + OH reaction were investigated by an experimental relative rate method and at the density functional theory level. ...Theoretical calculations for the addition reaction of OH to cis-3-hexene have also bee …
The kinetics of the cis-3-hexene + OH reaction were investigated by an experimental relative rate method and at the den …
Z-selective olefin metathesis processes catalyzed by a molybdenum hexaisopropylterphenoxide monopyrrolide complex.
Flook MM, Jiang AJ, Schrock RR, Müller P, Hoveyda AH. Flook MM, et al. J Am Chem Soc. 2009 Jun 17;131(23):7962-3. doi: 10.1021/ja902738u. J Am Chem Soc. 2009. PMID: 19462947 Free PMC article.
Z-Selectivity is also observed in the metathesis of cis-4-octene and cis-3-hexene by initiator 2a to give cis-3-heptene....
Z-Selectivity is also observed in the metathesis of cis-4-octene and cis-3-hexene by initiator 2a to give cis-3-heptene …
Evaluation of aroma enhancement for "Ecolly" dry white wines by mixed inoculation of selected Rhodotorula mucilaginosa and Saccharomyces cerevisiae.
Wang XC, Li AH, Dizy M, Ullah N, Sun WX, Tao YS. Wang XC, et al. Food Chem. 2017 Aug 1;228:550-559. doi: 10.1016/j.foodchem.2017.01.113. Epub 2017 Jan 25. Food Chem. 2017. PMID: 28317762
Mixed fermentation improved both the varietal and fermentative aroma compound composition, especially that of (Z)-3-hexene-1-ol, nerol oxide, certain acetates and ethyls group compounds. Citrus, sweet fruit, acid fruit, berry, and floral aroma traits were enh …
Mixed fermentation improved both the varietal and fermentative aroma compound composition, especially that of (Z)-3-hexene …
Hydroboration kinetics: Unusual kinetics for the reaction of 9-borabicyclo[3.3.1]nonane with representative alkenes.
Brown HC, Wang KK, Scouten CG. Brown HC, et al. Proc Natl Acad Sci U S A. 1980 Feb;77(2):698-702. doi: 10.1073/pnas.77.2.698. Proc Natl Acad Sci U S A. 1980. PMID: 16592773 Free PMC article.
For certain alkenes, such as 2-methyl-2-butene and cis-3-hexene, neither of the two steps is a decisive rate-determining step. Therefore, the reaction exhibits kinetic behavior between that of first- and three-halves-order kinetics....
For certain alkenes, such as 2-methyl-2-butene and cis-3-hexene, neither of the two steps is a decisive rate-determinin …
Gas-phase ozonolysis of alkenes: formation of OH from anti carbonyl oxides.
Kroll JH, Donahue NM, Cee VJ, Demerjian KL, Anderson JG. Kroll JH, et al. J Am Chem Soc. 2002 Jul 24;124(29):8518-9. doi: 10.1021/ja0266060. J Am Chem Soc. 2002. PMID: 12121079
OD is formed from both alkenes, indicating a pathway of hydroxyl-radical formation involving vinylic hydrogens, accounting for one-third of total OH formation from cis-3-hexene. The lack of a significant kinetic isotope effect suggests this pathway is the "ho …
OD is formed from both alkenes, indicating a pathway of hydroxyl-radical formation involving vinylic hydrogens, accounting for one-third of …
Benchmark Calculations for Bond Dissociation Enthalpies of Unsaturated Methyl Esters and the Bond Dissociation Enthalpies of Methyl Linolenate.
Li X, Xu X, You X, Truhlar DG. Li X, et al. J Phys Chem A. 2016 Jun 16;120(23):4025-36. doi: 10.1021/acs.jpca.6b02600. Epub 2016 Jun 1. J Phys Chem A. 2016. PMID: 27191950
In this study, we use Kohn-Sham density functional theory (DFT) and coupled cluster theory to calculate bond dissociation enthalpies (BDEs) of seven fragment molecules of methyl linolenate, in particular, propene, methyl formate, cis-3-hexene, 1,4-pentadiene, …
In this study, we use Kohn-Sham density functional theory (DFT) and coupled cluster theory to calculate bond dissociation enthalpies (BDEs) …
Identification and Quantification of Several Contaminated Compounds in Replacement Liquids of Electronic Cigarettes by Gas Chromatography-Mass Spectrometry.
Oh JA, Shin HS. Oh JA, et al. J Chromatogr Sci. 2015 Jul;53(6):841-8. doi: 10.1093/chromsci/bmu146. Epub 2014 Nov 16. J Chromatogr Sci. 2015. PMID: 25404560
Triethylene glycol, tetraethylene glycol and pentaethylene glycol were quantified in concentration ranges of 0.1-19.3 mg/L (10.5% detection frequency), 0.1-30.1 mg/L (12.4% detection frequency) and 0.1-24.9 mg/L (6.7% detection frequency) in the same samples. cis-3- …
Triethylene glycol, tetraethylene glycol and pentaethylene glycol were quantified in concentration ranges of 0.1-19.3 mg/L (10.5% detection …
A one-pot diastereoselective synthesis of cis-3-hexene-1,6-diols via an unusually reactive organozinc intermediate.
García C, Libra ER, Carroll PJ, Walsh PJ. García C, et al. J Am Chem Soc. 2003 Mar 19;125(11):3210-1. doi: 10.1021/ja029449d. J Am Chem Soc. 2003. PMID: 12630865
A highly diastereoselective method for the synthesis of cis-3-hexene-1,6-diols has been developed. This new reaction proceeds with excellent control of diastereoselectivity over four stereocenters and the double bond geometry. ...
A highly diastereoselective method for the synthesis of cis-3-hexene-1,6-diols has been developed. This new reaction pr …