Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Christopher J. Veal"'
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :3053-3058
The photochemistry of a series of β-thioacrylamides has been investigated. The acyclic compounds (9)–(12) undergo cis–trans isomerisation and cyclisation to oxazoles such as (13) and (21). The cyclic β-thioacrylamide (23) undergoes a π2s+π2s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfe2f238720ba79e40c4f0562d1e7ada
https://doi.org/10.1039/p19810003053
https://doi.org/10.1039/p19810003053
Autor:
Douglas W. Young, Christopher J. Veal
Publikováno v:
Chemischer Informationsdienst. 5
The product from the interesting rearrangement of penicillins with methyl chloroformate has been shown to have the structure and stereochemistry (X) by total stereospecific synthesis; this is in keeping with mechanistic considerations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eb69952a80e5b7724dca351332e665d
https://doi.org/10.1002/chin.197427260
https://doi.org/10.1002/chin.197427260
Autor:
CHRISTOPHER J. VEAL, DOUGLAS W. YOUNG
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b328bb71c8f66a5c5408be601ffad6b4
https://doi.org/10.1002/chin.197603359
https://doi.org/10.1002/chin.197603359
Publikováno v:
Chemischer Informationsdienst. 9
The dehydrovaline acrylamide (3) has been photolysed to yield the novel fused β-lactam system (4); this finding opens up a possible route to compounds which may be of interest in the light of current views on the mode of action of β-lactam antibiot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ec366c9d71dfb24d4d92e4a6e1baa73
https://doi.org/10.1002/chin.197805214
https://doi.org/10.1002/chin.197805214
Autor:
Christopher J. Veal, Douglas W. Young
Publikováno v:
Tetrahedron Letters. 17:2985-2986
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e81a9f76d8c23d8a54897b6094100acc
https://doi.org/10.1016/s0040-4039(01)85507-6
https://doi.org/10.1016/s0040-4039(01)85507-6
Autor:
Douglas W. Young, Christopher J. Veal
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2086
Separate stereospecific syntheses of the product [4-isopropylidene-2-(2-methylthio-1-phenylacetamidovinyl)-oxazol-5-(4H)-one] from the rearrangement of penicillin G with methyl chloroformate and of its geometric isomer have defined the former as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6cec289a181f198f3fa0f2d4eab1dca
https://doi.org/10.1039/p19750002086
https://doi.org/10.1039/p19750002086
Publikováno v:
J. Chem. Soc., Chem. Commun.. :678-678
The dehydrovaline acrylamide (3) has been photolysed to yield the novel fused β-lactam system (4); this finding opens up a possible route to compounds which may be of interest in the light of current views on the mode of action of β-lactam antibiot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1be9dc210e142c6bd89b1a45ad2b5e5
https://doi.org/10.1039/c39770000678
https://doi.org/10.1039/c39770000678
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65ee77b86aba30d3ce0a748dd3bb87e5
https://doi.org/10.1039/c39780000032
https://doi.org/10.1039/c39780000032
Autor:
Christopher J. Veal, Douglas W. Young
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :266
The product from the interesting rearrangement of penicillins with methyl chloroformate has been shown to have the structure and stereochemistry (X) by total stereospecific synthesis; this is in keeping with mechanistic considerations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b5c5ea4973ff23f44072dc6343306ce
https://doi.org/10.1039/c39740000266
https://doi.org/10.1039/c39740000266