Zobrazeno 1 - 10
of 29
pro vyhledávání: '"I. De Riggi"'
Autor:
I. De Riggi, M. P. Bertrand, Robert Nouguier, Stéphane Gastaldi, C. Lesueur, Carlos Jaime, Albert Virgili
Publikováno v:
The Journal of Organic Chemistry. 60:6040-6045
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18907289ef592804539feb981745b357
https://doi.org/10.1021/jo00124a012
https://doi.org/10.1021/jo00124a012
Publikováno v:
ChemInform. 24
The sulfonyl radical-promoted cyclizations of 1,6-unsymmetrical dienes can be totally chemoselective. The addition of tosyl halides to various 1,6-dienes bearing both a nucleophilic and an electrophilic double bond clearly indicates that the attracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::508ba3559c9e95aa7085c77258577c1f
https://doi.org/10.1002/chin.199310093
https://doi.org/10.1002/chin.199310093
Autor:
Robert Nouguier, Michèle P. Bertrand, A. Virgili, Carlos Jaime, I. De Riggi, Stéphane Gastaldi, C. Lesueur
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddef16e6fb4dbe7036e3c990b620af03
https://doi.org/10.1002/chin.199606086
https://doi.org/10.1002/chin.199606086
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cf23c7d8e38a30f76431b1760d02e9e
https://doi.org/10.1002/chin.199803083
https://doi.org/10.1002/chin.199803083
Publikováno v:
The Journal of Organic Chemistry. 57:6118-6125
The sulfonyl radical-promoted cyclizations of 1,6-unsymmetrical dienes can be totally chemoselective. The addition of tosyl halides to various 1,6-dienes bearing both a nucleophilic and an electrophilic double bond clearly indicates that the attracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::823abb0dff116316c160b5812f7424a9
https://doi.org/10.1021/jo00049a014
https://doi.org/10.1021/jo00049a014
Publikováno v:
Tetrahedron. 46:5285-5294
Addition of TsBr to diallyl malonates and allyl methallyl malonates is described. These cyclization reactions exhibit high stereoselectivity and very high regioselectivity. The structure of the reaction products is elucidated using 2D NMR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d81b66c9dcc1e76e3efc9eafc71d83dd
https://doi.org/10.1016/s0040-4020(01)87835-2
https://doi.org/10.1016/s0040-4020(01)87835-2
Publikováno v:
Biomedical chromatography : BMC. 15(3)
An improved methodology for microbatch screening in the liquid-solid enantioselective adsorption of racemates by solid chiral selector is presented and illustrated by the evaluation of a series of six cellulose tris(alpha-phenylpropionate) presenting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8f5f6bba41464c969d331c5c03babfd
https://pubmed.ncbi.nlm.nih.gov/11391673
https://pubmed.ncbi.nlm.nih.gov/11391673
Publikováno v:
Synfacts. 2011:0396-0396
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9b261cf0268b6bafda66ed53799bb76
https://doi.org/10.1055/s-0030-1259644
https://doi.org/10.1055/s-0030-1259644
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9895fa0f528c30ab8deae113da1bcbf6
https://doi.org/10.1002/chin.199048104
https://doi.org/10.1002/chin.199048104
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