Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Harriet A. Lindsay"'
Publikováno v:
Journal of Student Affairs Research and Practice. 59:324-337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff483d84a8bb5e0b5f05c97dc4930898
https://doi.org/10.1080/19496591.2021.1984932
https://doi.org/10.1080/19496591.2021.1984932
Publikováno v:
Polymer Bulletin. 79:5825-5842
Initial attempts to perform nearly bulk polymerization of bromoundecyl acrylate unexpectedly produced cross-linked gels, GelCH2Cl2 and GelDMF, exhibiting some interesting chemical features. Monomer concentrations were 50% by weight using methylene ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc0400c48a92142e7882776671825b8a
https://doi.org/10.1007/s00289-021-03768-w
https://doi.org/10.1007/s00289-021-03768-w
Publikováno v:
Tetrahedron. 65:10311-10316
The effects of C–C bond conformation, double bond geometry, and relative stereochemistry on the kinetic and thermodynamic stability of 30 iminium cations as they undergo an aza-Cope rearrangement have been examined via density functional calculatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53fbe76b456a8bcd34e515cbf50e95f7
https://doi.org/10.1016/j.tet.2009.10.010
https://doi.org/10.1016/j.tet.2009.10.010
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 806:223-230
The role of three structural variables on the stability of simple iminium cations has been examined via molecular orbital calculations. In general, the more stable conformation for the hydroxyl substituent is axial, and the more stable geometry for e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4790b2d90a648886e0942fcb9929aa72
https://doi.org/10.1016/j.theochem.2006.11.031
https://doi.org/10.1016/j.theochem.2006.11.031
Publikováno v:
Synthesis. 2007:902-910
We have developed a microwave-assisted aminolysis of epoxides as an efficient method for synthesizing a number of β-amino alcohols. In most cases, including in reactions of amines with a trisubstituted epoxide, only one equivalent of amine is requir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3e11bbd582efe45a19079001420eed
https://doi.org/10.1055/s-2007-965927
https://doi.org/10.1055/s-2007-965927
Publikováno v:
Tetrahedron. 58:2905-2928
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a978022ce7c070daacdad15e9a4ce8eb
https://doi.org/10.1016/s0040-4020(02)00164-3
https://doi.org/10.1016/s0040-4020(02)00164-3
Autor:
Gavin D. Jones, Silvana S. Dormi, Harriet A. Lindsay, John M. Hutchison, Matthias C. McIntosh, David A. Vicic
Publikováno v:
Organic Letters. 8:3663-3665
[reaction: see text] The synthesis of an advanced intermediate in the synthesis of the title compound has been achieved. Key steps include an Ireland-Claisen rearrangement to install the C7 tertiary alcohol stereocenter, an SN2' reaction of an alkoxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf93dfa868917853085d6f040daea0e
https://doi.org/10.1021/ol061072j
https://doi.org/10.1021/ol061072j
Publikováno v:
ChemInform. 33
A surprising and synthetically useful counterion-dependent reversal of diastereoselectivity was found in 1,2-additions of hard carbon nucleophiles to C6-heterosubstituted cyclohexenones. In general, Grignard reagents added syn to the C6-substituent a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3995df55a4661301f53cd00ad5e4a74
https://doi.org/10.1002/chin.200218093
https://doi.org/10.1002/chin.200218093
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f41972fcb203106fe58c102f8bfe6893
https://doi.org/10.1002/chin.200236045
https://doi.org/10.1002/chin.200236045
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd96ca0dbf5f262b1b14920efaeb026
https://doi.org/10.1002/chin.200233268
https://doi.org/10.1002/chin.200233268