Zobrazeno 1 - 10
of 12
pro vyhledávání: '"R. B. Deb‐Das"'
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63d6a998b87c558453c3b2c1fe904415
https://doi.org/10.1002/chin.199223157
https://doi.org/10.1002/chin.199223157
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6df3229d673a3fd845a8a1a4eb1fa361
https://doi.org/10.1002/chin.199237175
https://doi.org/10.1002/chin.199237175
Publikováno v:
ChemInform. 23
Two dihydro-β-carboline N-oxides undergo cycloaddition reactions with dimethyl acetylenedicar☐ylate and methyl propiolate: one of the cycloadducts can be converted to a fused pyrrolo-β-carboline by thermal rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9ba87d9a698b8926ae990a9126b2ac1
https://doi.org/10.1002/chin.199237210
https://doi.org/10.1002/chin.199237210
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec85bcaf9eea5bbb9208624b277c2f4
https://doi.org/10.1002/chin.199309148
https://doi.org/10.1002/chin.199309148
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a27db521f9ba8996e6a8153f38365d3a
https://doi.org/10.1002/chin.199336175
https://doi.org/10.1002/chin.199336175
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4fce73f284781e84b3732574048fbcf
https://doi.org/10.1002/chin.199407181
https://doi.org/10.1002/chin.199407181
Publikováno v:
Tetrahedron Letters. 33:839-840
Two dihydro-β-carboline N-oxides undergo cycloaddition reactions with dimethyl acetylenedicar☐ylate and methyl propiolate: one of the cycloadducts can be converted to a fused pyrrolo-β-carboline by thermal rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3992636be5e2eb1786fd64a1db8c9eaf
https://doi.org/10.1016/s0040-4039(00)77729-x
https://doi.org/10.1016/s0040-4039(00)77729-x
Publikováno v:
Australian Journal of Chemistry. 46:603
The N-allylindole-2-carbaldehydes (5)-(8) and related methyl ketones (9)-(12) undergo reaction with N- methylhydroxylamine to give the cycloadducts (14)-(17) and (19)-(22), respectively. These adducts contain isoxazolidine rings fused to pyrrolo [1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d205668a3d2c9b9ec28a17bdaacf1cc6
https://doi.org/10.1071/ch9930603
https://doi.org/10.1071/ch9930603
Nitrones and Oxaziridines. LXVII. Intermolecular Cycloaddition of Fused Indolyl Nitrone Ring Systems
Publikováno v:
Australian Journal of Chemistry. 46:1725
The two dihydro-β-carboline N-oxides (6) and (18) have been prepared by reductive cyclization of 2-acetyl-3-(β- nitroethyl ) indoles. These cyclic nitrones undergo 1,3-dipolar cycloaddition to alkynes to give the cycloadducts (21)-(25). Thermal rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a50855ee0e063a8e9e0097bddf143c35
https://doi.org/10.1071/ch9931725
https://doi.org/10.1071/ch9931725
Publikováno v:
Australian Journal of Chemistry. 45:1051
The 1-pyrroline 1-oxide (8) which contains an indol-7-yl substituent attached to the 2-position has been synthesized by reductive cyclization of the related γ -nitro ketone . The corresponding 1-pyrroline (9) has also been isolated as the result of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc558b6fef95a7b71996ba3df1326c39
https://doi.org/10.1071/ch9921051
https://doi.org/10.1071/ch9921051