Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mamoru Araki"'
Publikováno v:
Tetrahedron: Asymmetry. 9:157-167
Both enantiomers of C 2 -symmetric dimethyl 3,7-dihydroxybicyclo[3.3.0]-octa-2,6-diene-2,6-dicarboxylate 3 were prepared in enantiomerically pure form from symmetric tetraester 1 by the lipase-catalyzed demethoxycarbonylation, respectively. Double as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cee13e0d6b39248b4107f61b2409236e
https://doi.org/10.1016/s0957-4166(97)00616-2
https://doi.org/10.1016/s0957-4166(97)00616-2
Publikováno v:
Tetrahedron: Asymmetry. 6:31-34
σ-Symmetric bicyclic diketones 8a-c were enantioselectively reduced with baker's yeast to give the chiral hydroxy ketones 7a-c in 74–;100% ee. The reduction product (+)-7a and (−)-7′c were shown to be the chiral intermediates for the total syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29670b03332a8873ad48ace14d44c4b8
https://doi.org/10.1016/0957-4166(94)00344-b
https://doi.org/10.1016/0957-4166(94)00344-b
Publikováno v:
ChemInform. 26
σ-Symmetric bicyclic diketones 8a-c were enantioselectively reduced with baker's yeast to give the chiral hydroxy ketones 7a-c in 74–;100% ee. The reduction product (+)-7a and (−)-7′c were shown to be the chiral intermediates for the total syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3153e38fef6b2f591271db60505002
https://doi.org/10.1002/chin.199527237
https://doi.org/10.1002/chin.199527237
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e501f69c1c3505e54fa59d45995308ef
https://doi.org/10.1002/chin.199530086
https://doi.org/10.1002/chin.199530086
Publikováno v:
ChemInform. 29
Both enantiomers of C 2 -symmetric dimethyl 3,7-dihydroxybicyclo[3.3.0]-octa-2,6-diene-2,6-dicarboxylate 3 were prepared in enantiomerically pure form from symmetric tetraester 1 by the lipase-catalyzed demethoxycarbonylation, respectively. Double as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2fc0dece0cc1ea054b54f556be99b14
https://doi.org/10.1002/chin.199828044
https://doi.org/10.1002/chin.199828044
Publikováno v:
ChemInform. 29
The first asymmetric synthesis of (-)-isoiridomyrmecin and formal synthesis of (-)-loganin were done using chiral C2-symmetric building block dimethyl 3, 7-dihydroxy-cis-bicyclo[3.3.0]octa-2, 6-diene-2, 6-dicarboxylate (2) which was prepared by the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71eee83a2224f7f8db2969a02ba99183
https://doi.org/10.1002/chin.199844176
https://doi.org/10.1002/chin.199844176
Publikováno v:
Chemical and Pharmaceutical Bulletin. 46:736-738
The first asymmetric synthesis of (-)-isoiridomyrmecin and formal synthesis of (-)-loganin were done using chiral C2-symmetric building block dimethyl 3, 7-dihydroxy-cis-bicyclo[3.3.0]octa-2, 6-diene-2, 6-dicarboxylate (2) which was prepared by the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d8a082c0bb89ca04a27ed09c6730357
https://doi.org/10.1248/cpb.46.736
https://doi.org/10.1248/cpb.46.736
Autor:
Shinobu Sakurada, Tadashi Ogawa, Masaki Hagiwara, Tadanori Morikawa, Toru Okayama, Tetsuhisa Miyamae, Mamoru Araki
Publikováno v:
Chemicalpharmaceutical bulletin. 51(7)
To improve the oral bioavailability of a dermorphin tetrapeptide analog, N(alpha)-1-iminoethyl-Tyr-D-MetO-Phe-MebetaAla-OH (III), which has a potent analgesic activity after oral administration, various derivatives were synthesized to increase lipoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::533b7581d28ba57ef55c10fe6b46159d
https://pubmed.ncbi.nlm.nih.gov/12843580
https://pubmed.ncbi.nlm.nih.gov/12843580
Publikováno v:
Tetrahedron Letters. 36:2255-2256
Both enantiomers of C2-symmetric dimethyl 3,7-dioxo-cis-bicyclo[3.3.0]-octane-2,6-dicarboxylate (3) were prepared in enantiomerically pure form by the lipase-catalyzed demethoxycarbonylation, respectively. An expeditious formal total synthesis of (+)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9d70d9306dbd351b6d2555e92012ad9
https://doi.org/10.1016/0040-4039(95)00264-d
https://doi.org/10.1016/0040-4039(95)00264-d