Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D. W.-L. CHANG"'
Autor:
Eldon D. Megarity, A. K. Uriarte, Jack Saltiel, Alan D. Rousseau, Babu Thomas, D. W. L. Chang, Patrick Shannon
Publikováno v:
Pure and Applied Chemistry. 41:559-579
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a98a4f93b1611fdd95ce16ae2a41bc
https://doi.org/10.1351/pac197541040559
https://doi.org/10.1351/pac197541040559
Publikováno v:
Canadian Journal of Chemistry. 48:157-162
Irradiation of N-nitrosopiperidine and 3,3-dimethyl-1-butene in a Pyrex apparatus gave 3,3-dimethyl-1-piperidino-2-(N-nitrosohydroxylamino)butane as the major product, in contrast to similar additions to 1-hexene and other olefins. Depending on the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bfbae56714324b29a778c8b41eb2c0d
https://doi.org/10.1139/v70-022
https://doi.org/10.1139/v70-022
Publikováno v:
Canadian Journal of Chemistry. 48:1664-1669
In the presence of an acid, N-nitrosopiperidine photolytically adds to conjugated dienes to give 1:1 adducts in excellent yield. While the major products are the syn- and anti-isomers of piperidino α,β-unsaturated oxime derived from 1,4-addition, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbf56634c8a4212bcecdd03508ce3982
https://doi.org/10.1139/v70-275
https://doi.org/10.1139/v70-275
Publikováno v:
Canadian Journal of Chemistry. 49:3069-3071
The stereochemical course of the photoaddition of nitrosamines to a carbon–carbon double bond was shown to follow a free radical mechanism initiated by aminium radicals. The photoaddition to cyclohexene was highly stereoselective in which the adden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::368c2bb6acc1b0c2767195380d1442e5
https://doi.org/10.1139/v71-514
https://doi.org/10.1139/v71-514
Publikováno v:
Chemischer Informationsdienst. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaf06d95b507ca000e7c4f8c7f9d95f9
https://doi.org/10.1002/chin.198309120
https://doi.org/10.1002/chin.198309120
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55472f658eb3b69f5f3adeb89d51a339
https://doi.org/10.1002/chin.197936143
https://doi.org/10.1002/chin.197936143
Autor:
Y. L. Chow, D. W. L. Chang
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f570f28414eeb336fa45a1b9b0c8206
https://doi.org/10.1002/chin.197113330
https://doi.org/10.1002/chin.197113330
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6bc2b10c7428fd9fd714f0d2d8d48c19
https://doi.org/10.1002/chin.197041216
https://doi.org/10.1002/chin.197041216
Autor:
D. W. L. Chang, Y. L. Chow
Publikováno v:
Journal of the Chemical Society D: Chemical Communications. :64
Summary C-Nitroso-enamines are unstable intermediates generated during the photoaddition of N-nitrosopiperidine to an acetylene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8442c88f9833ec31bac7b7fb7cd700b8
https://doi.org/10.1039/c29710000064
https://doi.org/10.1039/c29710000064