Zobrazeno 1 - 4
of 4
pro vyhledávání: '"F. R. Leusink"'
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23bb8e4d2387049372217c1ea6e48b5e
https://doi.org/10.1002/chin.199303153
https://doi.org/10.1002/chin.199303153
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec29a6b90610cde5d4d8a28766cd427
https://doi.org/10.1002/chin.199648125
https://doi.org/10.1002/chin.199648125
Publikováno v:
Acta Crystallographica Section C: Crystal Structure Communications, 49, 826-828
The structure of rac-1-methyl-3-nitro{(1R,6S,8S)-6-phenyl-5, 8-(tetramethylene)tricyclo[3.2.1.0(2,7)]oct-3-eno}[4,3-b]pyrrole (1) has been determined. The compound, which is composed of a nitropyrrole annulated to a tricyclic octene, was prepared by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd02853855849ff43edf91e1c8938c45
https://doi.org/10.1107/s0108270192011156
https://doi.org/10.1107/s0108270192011156
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
