Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Robert Lalande"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 89:1039-1042
Acetonyl radicals created by action of di-t-butylperoxide on acetone (molar ratios acetone/acetylenic compound/DTBP = 20/1/0.2; 150°C; 3h) add to acetylenic compounds and lead to the formation of 1/1 adducts in low to moderate yields. 2/1 adducts ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9577d15a33d1cf81333ad747d574f9fd
https://doi.org/10.1002/bscb.19800891203
https://doi.org/10.1002/bscb.19800891203
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 88:677-682
Addition of acetonyl radicals to 1-octyne leads to the formation of 1/1 adducts. Besides the normal product, appear two kinds of cyclic derivatives. Formation of the latter is explained by hydrogen shifts in the transient vinyl radical. 1,5-hydrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de9819968180a89a3a078585dec83258
https://doi.org/10.1002/bscb.19790880907
https://doi.org/10.1002/bscb.19790880907
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 92:1011-1018
Free radical addition of propanal to double bonds, initiated by benzoyl peroxide, mainly leads to two adducts, an aldehyde and a ketone, when the double bond has a methylene group; these results are explained in terms of polar effects in the free rad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf47792fc5ea9e1e0047fe18723b179d
https://doi.org/10.1002/bscb.19830921110
https://doi.org/10.1002/bscb.19830921110
Autor:
Robert Lalande
Publikováno v:
Computer Music Journal. 19:105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f1278c1932c3d64838da8dc015312b5
https://doi.org/10.2307/3680604
https://doi.org/10.2307/3680604
Publikováno v:
Helvetica Chimica Acta. 67:149-159
The Free-Radical Decomposition of O,O-t-Butyl and O-Isopropenyl Peroxycarbonate in Solution: the Acetonylation of Esters, Acides and Nitriles The free-radical decomposition of O, O-t-butyl and O-isopropenyl peroxycarbonate in substratres possessing m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42acbce2e940b3e9748d0510c979f7b8
https://doi.org/10.1002/hlca.19840670118
https://doi.org/10.1002/hlca.19840670118
Isomerisation radicalaire de l'oxepanne. Un nouveau type de cyclisation homolytique sur un carbonyle
Publikováno v:
Tetrahedron Letters. 17:439-442
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::764f75c0c0e7fb9ad33f022e3931b646
https://doi.org/10.1016/s0040-4039(00)77874-9
https://doi.org/10.1016/s0040-4039(00)77874-9
Publikováno v:
Tetrahedron Letters. 10:745-748
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e5b97e8f1a4c41668ac2b3cbc18e71
https://doi.org/10.1016/s0040-4039(01)87798-4
https://doi.org/10.1016/s0040-4039(01)87798-4
Publikováno v:
Tetrahedron Letters. 13:1487-1490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::753c8c2b526c0cf559908a56b1837ab7
https://doi.org/10.1016/s0040-4039(01)84664-5
https://doi.org/10.1016/s0040-4039(01)84664-5
Publikováno v:
Journal of Heterocyclic Chemistry. 12:509-511
L'addition radicalaire du tetrahydrothiophene a des derives ethyleniques, sous amorcage peroxydique conduit a des tetrahydrothiophenes substitues en 2. Cette reaction semble etre une voie synthetique interessante de ces heterocycles. Di-t-butyl perox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87c4f3791fb075434884894b134fa7f4
https://doi.org/10.1002/jhet.5570120313
https://doi.org/10.1002/jhet.5570120313
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a92c9d84a06eda324ef718bc4c2eb79
https://doi.org/10.1002/chin.197432115
https://doi.org/10.1002/chin.197432115