Zobrazeno 1 - 10
of 34
pro vyhledávání: '"S. Fazal Hussain"'
Publikováno v:
Tetrahedron Letters. 21:4573-4576
The new aporphine-benzylisquinoline khyberine ( 4b ) is present in Berberis calliobotrys Aitch. ex Bienert in about one part per million. An effort is made to present a complete scheme for the biogenesis of aporphine-benylisoquinoline dimers which ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b1390b7590673abd94563c96644889
https://doi.org/10.1016/0040-4039(80)80076-1
https://doi.org/10.1016/0040-4039(80)80076-1
Publikováno v:
Tetrahedron. 34:635-640
The new isoquinoline alkaloid (−)-peshawarine ( 1 ) has been isolated from Hypecoum parviflorum Kar. & Kir. (Papaveraceae). Its synthesis in the racemic form from coptisine ( 6b ) involves a novel approach to cyclic hemiacetals in which the key ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b17838070f52dc6b5ba5edeebf21ab99
https://doi.org/10.1016/0040-4020(78)88096-x
https://doi.org/10.1016/0040-4020(78)88096-x
Publikováno v:
Journal of Natural Products. 44:169-178
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3ca9a232795b07bf2a5dd6c807f581
https://doi.org/10.1021/np50014a005
https://doi.org/10.1021/np50014a005
Autor:
S. Fazal Hussain, Maurice Shamma
Publikováno v:
Tetrahedron Letters. 21:3315-3318
Berberis orthobotrys produces the new dimer kalashine ( 1 ), together with the previously reported pakistanamine ( 2 ) and pakistanine ( 3 ). Kalashine is the first aporphine-benzylisoquinoline known to be substituted at C-11. Acid catalyzed rearrang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54963ab1acb2e5d98ddd4a54db928bea
https://doi.org/10.1016/s0040-4039(00)78677-1
https://doi.org/10.1016/s0040-4039(00)78677-1
Autor:
S. Fazal Hussain, Maurice Shamma
Publikováno v:
Tetrahedron Letters. 21:1909-1912
(+)-Parviflorine ( 1 ), found in Fumaria parviflora Lam. (Fumariaceae), is the first known glycosidic spirobenzylisoquinoline alkaloid. Its acid hydrolysis yields (+)-parfumine ( 4 ) and D-glucose. Klyne's rule indicates that 1 is a β-D-glucoside. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58a10ae36c2a59a76faea4b8de5eb68c
https://doi.org/10.1016/s0040-4039(00)93641-4
https://doi.org/10.1016/s0040-4039(00)93641-4
Publikováno v:
Journal of Natural Products. 46:251-255
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89b1fefd2b7e62410c51f16bd6ef3ca2
https://doi.org/10.1021/np50026a021
https://doi.org/10.1021/np50026a021
Publikováno v:
Journal of Natural Products. 49:488-493
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::106152d82929dd1c0928f188d49e9f0a
https://doi.org/10.1021/np50045a018
https://doi.org/10.1021/np50045a018
Publikováno v:
Tetrahedron Letters. 22:3127-3130
The dark yellow indenobenzazepine alkaloids lahorine ( 1 ) and lahoramine ( 2 ) have been found in Fumaria parviflora Lam. (Fumariaceae). In a transformation with biogenetic implications, treatment of the spirobenzylisoquinolines dihydrofumariline (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9e2538d7ff527d4adaf9ab339f485c9
https://doi.org/10.1016/s0040-4039(01)81844-x
https://doi.org/10.1016/s0040-4039(01)81844-x
Autor:
S. Fazal Hussain, Mekin Tanker, Gábor Blaskó, Natesan Murugesan, Bilge Sener, Maurice Shamma, Robert D. Minard
Publikováno v:
Tetrahedron Letters. 22:3135-3138
Fumarofine is not a spirobenzylisoquinoline. Rather, it is the first know reduced indenobensazepine alkaloid, and possesses the cis B/C fused structure 7 . Rearrangement of synthetic spirobensylisoquinoline 12 using methanesulfonyl chloride furnished
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1feac62d05303ceefe276d9417399dbe
https://doi.org/10.1016/s0040-4039(01)81846-3
https://doi.org/10.1016/s0040-4039(01)81846-3
Publikováno v:
Journal of Natural Products. 44:274-278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5b0791811311edd0690b223b4f913e1
https://doi.org/10.1021/np50015a006
https://doi.org/10.1021/np50015a006