Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ronald ten Have"'
Publikováno v:
The Journal of Organic Chemistry. 63:5332-5338
A series of 2-(trimethylstannyl)pyrroles 3, with substituents at the 3- and 4-positions, is synthesized efficiently by a base-induced reaction of stannylated TosMIC with Michael acceptors. Stille cross-couplings with bromobenzene and double cross-cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e55ca1bf266849871cd708a2d418497
https://doi.org/10.1021/jo972216y
https://doi.org/10.1021/jo972216y
Autor:
Ronald ten Have, Albert M. van Leusen
Publikováno v:
Tetrahedron. 54:1913-1920
3-Nitroindoles (10) are prepared in good yields via a thermal 6π-electrocyclization of 2,3-(dialkenyl)-4-nitropyrroles (4) in nitrobenzene, a solvent which causes in situ aromatization of the initially formed dihydroindoles (8). The corresponding re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1f875ba1df19edd00b00a3b0a773ad9
https://doi.org/10.1016/s0040-4020(97)10405-7
https://doi.org/10.1016/s0040-4020(97)10405-7
Publikováno v:
Tetrahedron, 53(33), 11355-11368. PERGAMON-ELSEVIER SCIENCE LTD
4(5)-Monosubstituted imidazoles (9) have been prepared via base-induced cycloaddition of tosylmethyl isocyanide (TosMIC) to N-(dimethylsulfamoyl)aldimines (2) or N-tosylaldimines (3). In the first case, N-(dimethylsulfamoyl)imidazoles 8 are the initi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce70faeb41546a6c4a97d2270778ccae
https://doi.org/10.1016/s0040-4020(97)00717-5
https://doi.org/10.1016/s0040-4020(97)00717-5
Publikováno v:
Synthetic Communications. 27:945-952
N-(Dimethylsulfamoyl)aldimines (3) a new type of shelf-stable aldimine derivatives, are readily prepared from aldehydes and N-(dimethylsulfamoyl)amide (2) in refluxing toluene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1055c2ad6975820956b514b2f04daa9
https://doi.org/10.1080/00397919708003037
https://doi.org/10.1080/00397919708003037
Publikováno v:
Synthesis-Stuttgart, 871-876. GEORG THIEME VERLAG KG
ISSUE=7;STARTPAGE=871;ENDPAGE=876;ISSN=0039-7881;TITLE=Synthesis-Stuttgart
ISSUE=7;STARTPAGE=871;ENDPAGE=876;ISSN=0039-7881;TITLE=Synthesis-Stuttgart
A series of 3(4)-nitropyrroles with alkenyl substituents in the 2- and 3-positions (or 3-position only) is synthesized efficiently in one operation by a base-induced addition of tosylmethyl isocyanide (TosMIC), or unsaturated homologs of TosMIC, to n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a643a1f83cdcf7eb894e21905e9c517
https://research.rug.nl/en/publications/3e48a8b0-63ba-4018-9a4b-d73d8aa236a5
https://research.rug.nl/en/publications/3e48a8b0-63ba-4018-9a4b-d73d8aa236a5
Publikováno v:
J. Chem. Soc., Chem. Commun.. :1401-1402
Three different approaches are described for the generation of derivatives of 2,3-dimethylene-2,3-dihydropyrrole 2, which are reactive intermediates in Diels–Alder cycloaddition reactions; one of the intramolecular cycloadditions provides a new tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6948fc156722466dc0420217ba94c60a
https://doi.org/10.1039/c39920001401
https://doi.org/10.1039/c39920001401
Publikováno v:
The Journal of Organic Chemistry. 64:2599-2599
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d854aafaeb15a736b24e2275b001ae7a
https://doi.org/10.1021/jo994000x
https://doi.org/10.1021/jo994000x
Publikováno v:
Journal of Organic Chemistry; 08/07/98, Vol. 63 Issue 16, p5332, 7p, 3 Diagrams, 3 Charts
Publikováno v:
Synthesis; January 1996, Vol. 1996 Issue: 7 p871-876, 6p
Autor:
KATE, RONALD TEN
Publikováno v:
Australian Motorcycle News; 5/1/2014, Vol. 63 Issue 21, p125-125, 1/6p