Zobrazeno 1 - 10
of 168
pro vyhledávání: '"G. D. MEAKINS"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d1e2485f6415ed3e1c52cbc53600359
https://doi.org/10.1002/chin.199128054
https://doi.org/10.1002/chin.199128054
Publikováno v:
ChemInform. 23
Reexamination of previous work and new studies show that the reactions of 2-aminothiazoles with (heterocyclic) aromatic aldehydes are not straightforward; there are wide divergencies in behaviour between the various amine-aldehyde pairs. Simple effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b173582612174bec05366182bd3752e6
https://doi.org/10.1002/chin.199212173
https://doi.org/10.1002/chin.199212173
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3f7b0613e838350e81928be53e79efb
https://doi.org/10.1002/chin.199348164
https://doi.org/10.1002/chin.199348164
Publikováno v:
Synthesis. 1991:621-624
Reexamination of previous work and new studies show that the reactions of 2-aminothiazoles with (heterocyclic) aromatic aldehydes are not straightforward; there are wide divergencies in behaviour between the various amine-aldehyde pairs. Simple effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::423d24f2dac873761150377cf17dfd7c
https://doi.org/10.1055/s-1991-26528
https://doi.org/10.1055/s-1991-26528
Autor:
H. C. Cowen, F. Riding, E. Warhurst, A. D. Buckingham, R. J. W. Le Fèvre, G. D. Meakins, R. N. Haszeldine, J. Jander, G. R. Clemo, B. W. Fox, Richard Raper, J. F. W. McOmie, I. M. White, O. L. Brady, P. E. Halstead, A. G. Sharpe, G. W. Gray, Brynmor Jones, J. Cast, T. S. Stevens, F. Bell, J. W. Cook, Leon Hunter, R. M. Barrer, N. Mackenzie, D. MacLeod, C. C. Barker, F. D. Casson, G. F. Laws, W. Carruthers, E. S. Lane, C. Williams
Publikováno v:
J. Chem. Soc.. :4168-4188
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cddac1fc66bf130c7299de251888327e
https://doi.org/10.1039/jr9530004168
https://doi.org/10.1039/jr9530004168
Autor:
D. E. Hathway, R. A. Shaw, M. Martin-Smith, Y. Pocker, G. D. Meakins, J. S. Stephenson, H. J. Emeléus, J. D. Smith, R. J. W. Cremlyn, G. W. Kenner, J. Mather, Alexander Todd, D. F. Downing, D. Woodcock, E. Boyland, D. Manson, A. S. Dunn, A. Hanrahan, B. G. Gowenlock, P. Pritchard Jones, D. W. Ovenall, I. T. Millar, C. T. Mortimer, H. D. Springall
Publikováno v:
J. Chem. Soc.. :520-536
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03dac3f687cae651dc472db6bfe4c2bb
https://doi.org/10.1039/jr9580000520
https://doi.org/10.1039/jr9580000520
Publikováno v:
J. Chem. Soc. C. :2674-2682
Twenty-eight vicinal cholestanediols (positions 1,2; 2,3; 3,4; 4,5; 5,6; 6,7; and 7,8) have been prepared by unambiguous routes starting from the corresponding olefins. The O–H stretching bands of dilute solutions of these diols and of seven refere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26e1e6111d4af20b2941b600852271b0
https://doi.org/10.1039/j39680002674
https://doi.org/10.1039/j39680002674
Autor:
P. C. Cherry, J. E. Bridgeman, G. D. Meakins, V. Kumar, E. E. Richards, Y. Morisawa, A. S. Clegg, J. M. Evans, Ewart R. H. Jones, A. Kasal, P. D. Woodgate
Publikováno v:
J. Chem. Soc. C. :250-257
Structural investigation of the products obtained by microbiological hydroxylation of substrates in the androstane, pregnane, and œstrane series has involved examining the 1H n.m.r. spectra of 344 steroids, 243 of them being new compounds. Mild oxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed1e2b221e8e9d7a6cd75c3b1a96362
https://doi.org/10.1039/j39700000250
https://doi.org/10.1039/j39700000250
Publikováno v:
J. Chem. Soc. C. :2841-2844
O-Substituted glycollic esters (R1O·CH2·CO2R2) are readily prepared by treating hydroxy-steroids (R 1OH) with alkyl diazoacetates in the presence of fluoroboric acid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33fb5a8174a090658e1282f7a3677bd4
https://doi.org/10.1039/j39680002841
https://doi.org/10.1039/j39680002841
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :499-502
The following new compounds have been prepared: 2α-, 4α-, 4β-, 6β- and12α-hydroxy-5α-androstanes; the acetates of these alcohols and of the 1α-, 1β-, 2β-, 6α-, 12β-, 15α- and 15β-hydroxy-5α-androstanes; 3α- and 3β-hydroxy-5α-androst-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64c4d995595069f6bd9fb9fb417abd2f
https://doi.org/10.1039/p19720000499
https://doi.org/10.1039/p19720000499