Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Adari B. Rao"'
Publikováno v:
International Journal of Food Science & Technology. 47:2554-2560
Summary The food industry has traditionally used sugar (sucrose) as a sweetening agent; however the dietary and health demands are continuing to expand the market for sweeteners as an alternative to sucrose. The leaves of Stevia rebaudiana are rich s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c8d5f167b1277cc1dcedbda23f72825
https://doi.org/10.1111/j.1365-2621.2012.03134.x
https://doi.org/10.1111/j.1365-2621.2012.03134.x
Publikováno v:
ChemInform. 22
o-Cyanophenyl allyl carbamate (3), 3-allyl-3,4-dihydro-4-imino-2H-1,3-benzoxazine-2-thione (8a), and -quinazoline-2(1H)-thiones (8b–d) have been cyclized to 2,3-dihydro-2-methyl-5H-imidazo[1,2-c][1,3]benzoxazin-5-one (5), the corresponding 5-thione
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c239ddb34b310a2b4f08f12b935fbbd4
https://doi.org/10.1002/chin.199102094
https://doi.org/10.1002/chin.199102094
Publikováno v:
Tetrahedron Letters. 33:4077-4080
Stereoselective synthesis of 2-(S)-propanol amines by the ring-opening of racemic epoxides with arylamines in presence of rat liver microsomes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0927a9d6c25959e869383318c017769
https://doi.org/10.1016/0040-4039(92)88104-d
https://doi.org/10.1016/0040-4039(92)88104-d
Stereoselective metabolism of 3-isopropyl-5-(1-naphthoxymethyl)oxazolidine, a prodrug of propranolol
Publikováno v:
Biochemical pharmacology. 41(9)
This investigation suggests that the oxazolidine derivative of propranolol is a prodrug which is hydrolysed stereoselectively to propranolol by hepatic post-mitochondrial supernatant. The (S)-form of the prodrug is more stable in the biological syste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d41eb79fdf74e14358d9b6bb655fe71
https://pubmed.ncbi.nlm.nih.gov/2018570
https://pubmed.ncbi.nlm.nih.gov/2018570
Publikováno v:
Chemistry Letters. 19:655-656
The enzymatic conversion of aryl allylthiocarbamates and 1-allyl-3-arylthioureas by baker’s yeast to the corresponding carbamates and ureas in good yields is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe41618b13a77a070d7f441647b8bd80
https://doi.org/10.1246/cl.1990.655
https://doi.org/10.1246/cl.1990.655
Publikováno v:
HETEROCYCLES. 31:577
An approach to the synthesis of 4-imino substituted 1,3-benzoxazin-2-ones, 1,2,3-benzoxathiazin-2-ones and 2-quinazolinones based on the enzymatic cyclisation of the labile-functionalized compounds with ultrasonically baker's yeast.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00ffe948281663c0af055bd905ba71f8
https://doi.org/10.3987/com-89-5307
https://doi.org/10.3987/com-89-5307
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2755
o-Cyanophenyl allyl carbamate (3), 3-allyl-3,4-dihydro-4-imino-2H-1,3-benzoxazine-2-thione (8a), and -quinazoline-2(1H)-thiones (8b–d) have been cyclized to 2,3-dihydro-2-methyl-5H-imidazo[1,2-c][1,3]benzoxazin-5-one (5), the corresponding 5-thione
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21041e5f6e6880f30a4f21173c61b2b9
https://doi.org/10.1039/p19900002755
https://doi.org/10.1039/p19900002755
Publikováno v:
European Journal of Medicinal Chemistry. 23:487-489
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60ff80c40415e6a5967af6c4fdc340d8
https://doi.org/10.1016/0223-5234(88)90148-1
https://doi.org/10.1016/0223-5234(88)90148-1