Zobrazeno 1 - 10
of 14
pro vyhledávání: '"B. Kopping"'
Publikováno v:
ChemInform. 22
Tris(trimethylsilyl)silane is an effective mediator for the formation of carbon-carbon bonds via radicals using alkyl isocyanides as precursors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d89c8cd4dcd884102f611909dbce5c89
https://doi.org/10.1002/chin.199140096
https://doi.org/10.1002/chin.199140096
Autor:
Bernd Giese, D. Griller, Chryssostomos Chatgilialoglu, K. B. Clark, B. Kopping, Marco Ballestri
Publikováno v:
ChemInform. 22
Tris(trimethylsily1)silane is an effective reducing agent for organic halides, selenides, xanthatee, and isocyanide, as well as an effective hydrosilylating agent for dialkyl ketones and alkenes. The silane functions as a mediator in the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34f82fca91f679cebe4a7348fe22d8e0
https://doi.org/10.1002/chin.199131104
https://doi.org/10.1002/chin.199131104
Publikováno v:
ChemInform. 27
Radical cyclization reactions are among the most powerful and versatile methods for the construction of mono- and polycyclic systems. The advantages these reactions offer to the synthetic organic chemist include high functional group tolerance and mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9256cd0bd940bc2bb4d91d27714ba736
https://doi.org/10.1002/chin.199640274
https://doi.org/10.1002/chin.199640274
Publikováno v:
The Journal of Organic Chemistry. 57:3994-4000
tris(trimethylsilyl)silane adds across the double bond of a variety of mono-, di-, and trisubstituted under free-radical conditions in good yields. The reaction, which proceeds via a free-radical chain mechanim, is highly regioselective (anti-Markovn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8230546380af8faf0a06fcbac10c2693
https://doi.org/10.1021/jo00040a048
https://doi.org/10.1021/jo00040a048
Publikováno v:
Tetrahedron Letters. 31:6013-6016
Tris(trimethylsilyl)silane is an effective mediator for the formation of carbon-carbon bonds via radicals using alkyl isocyanides as precursors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ec04a621dce71861cb1b555267a0fae
https://doi.org/10.1016/s0040-4039(00)98016-x
https://doi.org/10.1016/s0040-4039(00)98016-x
Publikováno v:
Organic Reactions ISBN: 0471264180
Radical cyclization reactions are among the most powerful and versatile methods for the construction of mono- and polycyclic systems. The advantages these reactions offer to the synthetic organic chemist include high functional group tolerance and mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8da2684222b1b4a3f2c75a61d4318809
https://doi.org/10.1002/0471264180.or048.02
https://doi.org/10.1002/0471264180.or048.02
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::228592f9c2db1ac23b369ba9f8878e6a
https://doi.org/10.1002/chin.199251225
https://doi.org/10.1002/chin.199251225
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c08f6b50296cddb3c46f806233c7eecf
https://doi.org/10.1002/chin.198932294
https://doi.org/10.1002/chin.198932294
Autor:
Marco Ballestri, B. Kopping, Chryssostomos Chatgilialoglu, K. B. Clark, D. Griller, Bernd Giese
Publikováno v:
Scopus-Elsevier
Tris(trimethylsily1)silane is an effective reducing agent for organic halides, selenides, xanthatee, and isocyanide, as well as an effective hydrosilylating agent for dialkyl ketones and alkenes. The silane functions as a mediator in the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::671299212c55f98fc746bc690f1c61c4
http://www.scopus.com/inward/record.url?eid=2-s2.0-0001044552&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0001044552&partnerID=MN8TOARS
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