Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Chitra Adams"'
Autor:
Chitra Adams, David Reginald Adams
Publikováno v:
Synthetic Communications. 20:469-475
A simple synthesis of 2-cyano-3-dimethylamino-N-(aryl)-acrylamides and their subsequent conversion to 2-chloro-3-cyano-quinclines is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b8459db57f042c1e0f450eba83dc55
https://doi.org/10.1080/00397919008052789
https://doi.org/10.1080/00397919008052789
Autor:
David Reginald Adams, Chitra Adams
Publikováno v:
ChemInform. 21
A simple synthesis of 2-cyano-3-dimethylamino-N-(aryl)-acrylamides and their subsequent conversion to 2-chloro-3-cyano-quinclines is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03e1aa83d206a700b5aef7ff7eccee21
https://doi.org/10.1002/chin.199034163
https://doi.org/10.1002/chin.199034163
Autor:
Chitra Adams
Publikováno v:
Synthetic Communications. 14:1349-1353
Sodium borohydride in Dimethyl Sulphoxide in the presence of added metal salts selectively reduces aldehydes in the presence of ketones and converts α,β -unsaturated ketones to the corresponding unsaturated alcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::708651ca214923ea03d728eb09845d61
https://doi.org/10.1080/00397918408057674
https://doi.org/10.1080/00397918408057674
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1466
Rate measurements are reported for the reduction of acetone pivalaldehyde, and benzaldehyde by sodium and tetramethylammonium tetrahydridoborates in dimethyl–sulphoxide–water systems, some containing a low concentration of sodium hydroxide to imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea48707e91499ea5bf84a6c2d62657af
https://doi.org/10.1039/p29770001466
https://doi.org/10.1039/p29770001466
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :182
Hydrogen exchange has been observed between tritiated sodium borohydride and the aldehyde group of benzaldehyde, and is interpreted as due to a reverse hydride transfer (as a cage reaction) between borane and benzoxide ion, the primary products of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84d5317d4124dc69764ee52755cf7a48
https://doi.org/10.1039/c39770000182
https://doi.org/10.1039/c39770000182
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1767
The products of controlled-potential electrolysis of cis- and trans-diacetoxystilbene are dependent on solvent composition; in dry dimethylformamide the major product is diphenylacetylene (formed by reductive elimination) whereas in aqueous dimethylf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd89fec2367af487fe55c4e19241d5d6
https://doi.org/10.1039/p29790001767
https://doi.org/10.1039/p29790001767
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1472
The reduction of benzaldehyde by tritiated sodium tetrahydridoborate in dimethyl sulphoxide and dimethyl sulphoxide–water mixtures as solvents is accompanied by the incorporation of tritium into the aldehyde group of unchanged benzaldehyde. The occ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::510f023ff9f3a8a41130abfe5f31c04e
https://doi.org/10.1039/p29770001472
https://doi.org/10.1039/p29770001472
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :353
Efficient anodic mono- and di-acetoxylation of methyl oleate is described. Acetoxylation is consecutive and conditions may be adjusted to give a maximum of either 60% monoacetoxylation or 85% diacetoxylation. Both mono- and di-substituted products ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daa025863068634fb50732d79b67ccc2
https://doi.org/10.1039/p19790000353
https://doi.org/10.1039/p19790000353
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1071
For 1,2,4-trimethylcyclohexene-4-carboxylic acid voltammetric experiments and controlled potential electrolysis are used to show that the carbon–carbon double bond is more readily oxidised than the carboxylate function. Electro-oxidation in aqueous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::182379aae32aa5c865c5a42afdc31690
https://doi.org/10.1039/p29780001071
https://doi.org/10.1039/p29780001071
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1 (0300922X); 1979, p353-356, 4p