Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tetsuji Yata"'
Publikováno v:
Chemistry – A European Journal. 28
Strong main-group Lewis acids such as silylium ions are known to effectively promote heterolytic C(sp3)-F bond cleavage. However, carrying out the C(sp2)-F bond transformation of vinylic C- F bonds has remained an unmet challenge. Herein, we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::006fa7960cf002208741140912c1e88f
https://doi.org/10.1002/chem.202103852
https://doi.org/10.1002/chem.202103852
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(7)
Strong main-group Lewis acids such as silylium ions are known to effectively promote heterolytic C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::097f4ed90d4de426341eb594b2177988
https://pubmed.ncbi.nlm.nih.gov/34837264
https://pubmed.ncbi.nlm.nih.gov/34837264
Publikováno v:
The Journal of Organic Chemistry. 84:14330-14341
The oxyindation of carbonyl-ene-yne compounds with indium trihalides proceeded efficiently to give di-, tri-, and tetrasubstituted 2-pyrones bearing a carbon-indium bond. The metalated 2-pyrone and a zwitterion intermediate were identified by X-ray c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b390f8a54e2d00e3b48486317e42bbf
https://doi.org/10.1021/acs.joc.9b02186
https://doi.org/10.1021/acs.joc.9b02186
Publikováno v:
The Journal of Organic Chemistry. 83:740-753
Hydrofunctionalization is one of the most important transformation reactions of alkenes. Herein, we describe the development of an indium-triiodide-catalyzed hydrofunctionalization of alkenes bearing a hydroxy group using various types of organosilic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd8cf460b18d296101f774159b1e857
https://doi.org/10.1021/acs.joc.7b02739
https://doi.org/10.1021/acs.joc.7b02739
Publikováno v:
Chemical Science. 9:6041-6052
The cyclization of heteroatom-containing alkynes with π acidic metal salts is an attractive method to prepare heterocycles because the starting materials are readily available and the organometallic compounds are useful synthetic intermediates. A ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc9b30a4dd824e69674289943a75c29f
https://doi.org/10.1039/c8sc01537f
https://doi.org/10.1039/c8sc01537f
Publikováno v:
Chemistry – A European Journal. 27:8232-8232
Fluorinated heterocycles have attracted much attention in the pharmaceutical and agrochemical industries. Many strategies have already been developed to achieve the synthesis of fluorinated heterocycles. Formidable challenges remain, however, in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75163e735e94376d8b236176b4af48f5
https://doi.org/10.1002/chem.202101570
https://doi.org/10.1002/chem.202101570
Publikováno v:
Chemistry – A European Journal. 27:8228-8228
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c20560fa66abbe505272c9d808fd0214
https://doi.org/10.1002/chem.202101569
https://doi.org/10.1002/chem.202101569
Publikováno v:
Chemical Science
The oxymetalation of terminal alkynes proceeded in a 6-endo cyclization manner with the use of indium or gallium trihalide.
The cyclization of heteroatom-containing alkynes with π acidic metal salts is an attractive method to prepare heterocycl
The cyclization of heteroatom-containing alkynes with π acidic metal salts is an attractive method to prepare heterocycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d03ffe8282c0547a1b5267ca9a2ac2b
https://pubmed.ncbi.nlm.nih.gov/30079217
https://pubmed.ncbi.nlm.nih.gov/30079217
Publikováno v:
Journal of Organic Chemistry; 1/19/2018, Vol. 83 Issue 2, p740-753, 14p