Zobrazeno 1 - 10
of 30
pro vyhledávání: '"E. Bernocchi"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c563f7af0ea65e6afbd6c5a27496ec6
https://doi.org/10.1002/chin.199121155
https://doi.org/10.1002/chin.199121155
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b65b5d90ebd755b8b9629a9991f39620
https://doi.org/10.1002/chin.199107220
https://doi.org/10.1002/chin.199107220
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::916495c733654d0134572c769f2aca8f
https://doi.org/10.1002/chin.199126257
https://doi.org/10.1002/chin.199126257
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f137a1cdcc8b5f38ffc000f2eeebe230
https://doi.org/10.1002/chin.199121106
https://doi.org/10.1002/chin.199121106
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47e5468b4d4a44993887717597347102
https://doi.org/10.1002/chin.199248121
https://doi.org/10.1002/chin.199248121
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fbad27a8142bfe5a8c1bb0c25185120
https://doi.org/10.1002/chin.199235207
https://doi.org/10.1002/chin.199235207
Publikováno v:
Tetrahedron Letters. 33:3073-3076
Heck-type reactions involving enol triflates 1 and allylic alcohols 2 result in the formation of conjugated dienols as the major products. The regioselectivity for substitution at the terminal carbon of the alcohol is generally good and dienols 3 can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d2d0a8cebcd7050679bb0526682a329
https://doi.org/10.1016/s0040-4039(00)79603-1
https://doi.org/10.1016/s0040-4039(00)79603-1
Publikováno v:
Synlett. 1992:161-164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1f9736d12ba3a4bfdde8987408b948b
https://doi.org/10.1055/s-1992-21303
https://doi.org/10.1055/s-1992-21303
Publikováno v:
Tetrahedron Letters. 31:2463-2466
E-Allylamines N-protected with the easily removable tert-butoxycarbonyl group are stereoselectively prepared in good to high yield through the palladium-catalysed reaction of vinyl triflates with N,N-di-tert-butoxycarbonyl-N-allylamine in the presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4c034de47fbe692ef7a73f216b47ce3
https://doi.org/10.1016/s0040-4039(00)97390-8
https://doi.org/10.1016/s0040-4039(00)97390-8
The palladium-catalysed reaction of vinyl triflates with Z-2-buten-1,4-diol affords β-vinyl-γ-butyrolactols (4-vinyl-2-hydroxy-tetrahydrofurans) which are converted into the corresponding β-vinyl-γ-butyrolactones by a smooth oxidation with Ag2CO3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47cbd9117f08a9a8e7924b00d55947f7
http://hdl.handle.net/11697/8552
http://hdl.handle.net/11697/8552
