Zobrazeno 1 - 10
of 419
pro vyhledávání: '"J. Cymerman Craig"'
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 88:1012-1018
A method involving the combined use of ORD and CD is described by which both the relative and absolute configuration of the two asymmetric centres in amino alcohols, containing only the amino and hydroxyl chromophores, may be determined. Application
Publikováno v:
Chirality. 10:169-172
Circular dichroism (CD) spectra were determined for the bioactive (+)-enantiomers of 1 · HCl, 3 · HCl, and 4 · HBr to characterize the chiroptical properties of these pyrroloisoquinoline antidepressants. The compounds showed a low-intensity negati
Autor:
J. Cymerman Craig, M. Aslam Ansari
Publikováno v:
Synthetic Communications. 26:1789-1792
An improved protocol for the oxidation of sec. alcohols by copper permanganate is described by carrying out the reaction in a homogeneous medium (acetic acid), affording rapid and complete conversion to the ketones.
Autor:
M. Aslam Ansari, J. Cymerman Craig
Publikováno v:
Synthetic Communications. 21:1971-1979
The novel reagent tetramethylammonium glycinate has been introduced as the most effective glycine derivative for the convenient synthesis of 4, 5, 6, 7-tetrahydroisoindoles (orpyrroles unsubstituted in the 2 and 5 positions) from 1,3-dicarbonyl compo
Autor:
E. Thomas Everhart, J. Cymerman Craig
Publikováno v:
Synthetic Communications. 20:2147-2150
Polar alcohols obtained from their β-(trimethylsilyl) ethoxymethyl (SEM) ethers by deprotection using the tetra-n-butylammonium fluoride reagent, can be efficiently isolated after quantitative removal of the excess reagent as the insoluble tetra-n-b
Autor:
J. Cymerman Craig, Aslam M. Ansari
Publikováno v:
Synthesis. 1995:147-149
Publikováno v:
Organic Syntheses
α-Naphthyl isothiocyanate reactant: 16.2 g. (0.08 mole) of dry α-naphthylthiourea product: α-naphthyl isothiocyanate product: phenyl product: o-chlorophenyl product: p-bromophenyl product: p-biphenylyl product: β-naphthyl product: 9-phenanthryl p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff1a36d7b5c52567bb5ea3f74a2f5d49
https://doi.org/10.1002/0471264180.os036.22
https://doi.org/10.1002/0471264180.os036.22
Autor:
J. Cymerman‐Craig, J. W. Loder
Publikováno v:
Organic Syntheses
Methyl 2-thienyl sulfide product: methyl 2-thienyl sulfide Keywords: Grignard and related reactions; sulfur, purification of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8683f7b90be7cb7a0b3a30889a1a5d64
https://doi.org/10.1002/0471264180.os035.30
https://doi.org/10.1002/0471264180.os035.30