Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aswinkumar Garimallaprabhakaran"'
Publikováno v:
ARKIVOC, Vol 2012, Iss 6, Pp 119-128 (2012)
Externí odkaz:
https://doaj.org/article/7dc8c9fe925b432bb703bde54380bacc
Autor:
Pinguan Zheng, Peter R. Schreiner, Parham Rooshenas, Aswinkumar Garimallaprabhakaran, Michael Harmata, Zhengxin Cai
Publikováno v:
European Journal of Organic Chemistry. 2011:5255-5260
Treatment of [2-(2-bromophenyl)allyl]trimethylsilane with tBuLi in THF at –78 °C resulted in the rapid migration of the trimethylsilyl group to afford an allylic organolithium that can be easily trapped by a wide range of electrophiles. This is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1bcf470a4b4fb16f120129b1f6fd928
https://doi.org/10.1002/ejoc.201100783
https://doi.org/10.1002/ejoc.201100783
Publikováno v:
Synlett. 2011:361-364
The N-acylation of a sulfoximine with carboxylic acids was accomplishedwith boric acid and several boronic acids. Aliphatic acids givefair yields of products while acids related to phenylacetic andphenoxyacetic acids perform much better. Aromatic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be118bc04bf26f1168c92f5fe9973e1
https://doi.org/10.1055/s-0030-1259328
https://doi.org/10.1055/s-0030-1259328
Autor:
Zhengxin Cai, Peter R. Schreiner, Aswinkumar Garimallaprabhakaran, Michael Harmata, Parham Rooshenas, Pinguan Zheng
Publikováno v:
ChemInform. 43
Treatment of [2-(2-bromophenyl)allyl]trimethylsilane with tBuLi in THF at –78 °C resulted in the rapid migration of the trimethylsilyl group to afford an allylic organolithium that can be easily trapped by a wide range of electrophiles. This is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29a78a6a4dae09be0d8dc1b8796957c1
https://doi.org/10.1002/chin.201207034
https://doi.org/10.1002/chin.201207034
Publikováno v:
ChemInform. 42
Boric acid reacts with carboxylic acids to form reactive acylating agents which are intercepted by sulfoximes (I).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::874e9646a12b59117f6d314bdd5bf74e
https://doi.org/10.1002/chin.201123071
https://doi.org/10.1002/chin.201123071