Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Martin A. C. Button"'
Publikováno v:
Journal of Heterocyclic Chemistry. 37:1505-1510
3-Aryl-5-(benzotriazol-1-ylmethyl)- 10a-f and 3-p-methoxyphenyl-5-(α-benzotriazol-1-yl-α-ethoxymethyl)-isoxazole (13) were prepared in high yields by 1,3-dipolar cycloadditions of 1-propargyl-benzotriazole (5) and (α-ethoxypropargyl)benzotriazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd6a72b2e5ab64727919b65fe0a4c960
https://doi.org/10.1002/jhet.5570370616
https://doi.org/10.1002/jhet.5570370616
Autor:
Martin A. C. Button, Steven M. Allin
Publikováno v:
Tetrahedron Letters. 39:3345-3348
The anionic amino-Cope rearrangement of suitably functionalized acyclic 3-amino-1,5-diene substrates has been achieved and we report the first example of an asymmetric anionic amino-Cope rearrangement to yield an enantiomerically enriched product (75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e65cdc63200f37409466ba374f3cd8bd
https://doi.org/10.1016/s0040-4039(98)00487-0
https://doi.org/10.1016/s0040-4039(98)00487-0
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5662493d37ed080b4181c80e2bbc57a
https://doi.org/10.1002/chin.199749083
https://doi.org/10.1002/chin.199749083
Autor:
Martin A. C. Button, Steven M. Allin
Publikováno v:
ChemInform. 29
The anionic amino-Cope rearrangement of suitably functionalized acyclic 3-amino-1,5-diene substrates has been achieved and we report the first example of an asymmetric anionic amino-Cope rearrangement to yield an enantiomerically enriched product (75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9387ad6e9f69dada036c345436671361
https://doi.org/10.1002/chin.199830098
https://doi.org/10.1002/chin.199830098
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ed5170dd73f4f24703a379a7b7eedb3
https://doi.org/10.1002/chin.199904040
https://doi.org/10.1002/chin.199904040
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e90c80e8c529c0de2a7e87be0d4ec4c8
https://doi.org/10.1002/chin.200123121
https://doi.org/10.1002/chin.200123121
Publikováno v:
ChemInform. 32
3-Aryl-5-(benzotriazol-1-ylmethyl)- 10a-f and 3-p-methoxyphenyl-5-(α-benzotriazol-1-yl-α-ethoxymethyl)-isoxazole (13) were prepared in high yields by 1,3-dipolar cycloadditions of 1-propargyl-benzotriazole (5) and (α-ethoxypropargyl)benzotriazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51365d54afd2d8e87f390832407a5b2d
https://doi.org/10.1002/chin.200123115
https://doi.org/10.1002/chin.200123115
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::763de51e9ca94c9eca626ce035d30fbb
https://doi.org/10.1002/chin.200136095
https://doi.org/10.1002/chin.200136095
Autor:
Alan R. Katritzky, Martin A. C. Button
Publikováno v:
ChemInform. 32
α-(Benzotriazolyl)methyl thioethers 1a−e reacted with styrenes under Lewis acid catalysis to give novel polysubstituted thiochromans (3,4-dihydro-2H-1-benzothiopyrans) 3−14 and 16−20 in generally high yields. Most thiochromans were isolated as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a5b21447336729fd99b36610c07bf07
https://doi.org/10.1002/chin.200148043
https://doi.org/10.1002/chin.200148043
Publikováno v:
Synlett. 1998:1117-1119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa5cfa8896f6a995a0336af4726913da
https://doi.org/10.1055/s-1998-1880
https://doi.org/10.1055/s-1998-1880