Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Indanomycin"'
Publikováno v:
European Journal of Organic Chemistry. 2020:1947-1955
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4300d1822282390f0ef2d196773891b8
https://doi.org/10.1002/ejoc.202000156
https://doi.org/10.1002/ejoc.202000156
Autor:
Xiao-Yuan Lian, Zhizhen Zhang
Publikováno v:
Natural product research. 27(23)
Four indanomycin-related antibiotics 2–5 were isolated from the cultured broth of marine Streptomyces antibioticus strain PTZ0016. Their structures were characterised as 16-deethylindanomycin (2), iso-16-deethylindanomycin (3), 16-deethylindanomyci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9851468d72ff67ec78a4afcb62eef07
https://pubmed.ncbi.nlm.nih.gov/23639115
https://pubmed.ncbi.nlm.nih.gov/23639115
Publikováno v:
Organic letters. 13(10)
The indanomycin biosynthetic gene (idm) cluster was recently identified from Streptomyces antibioticus NRRL 8167. The disruption of one of these genes, idmH, and the increased production of a previously unreported metabolite in this mutant is reporte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::659a81b6de32115c0cc013d6247ae3af
https://pubmed.ncbi.nlm.nih.gov/21491871
https://pubmed.ncbi.nlm.nih.gov/21491871
Autor:
David M. Armistead, K. Shankaran, Steven D. Burke, M. H. Parker, Kort Michael E, Mark A. Matulenko, A. D. Piscopio
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee6956ac6505f0d2594b15197415ecdd
https://doi.org/10.1002/chin.199423265
https://doi.org/10.1002/chin.199423265
Autor:
Wendy L. Kelly, Kathryn E. Roege
Publikováno v:
Organic letters. 11(2)
The pyrroloketoindane antibiotic indanomycin is produced by Streptomyces antibioticus NRRL 8167. These hybrid nonribosomal peptide-polyketide ionophore antibiotics are characterized by the presence of an unusual indane ring system, and there is inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b79f81037fc34050cf8bb429dbabcdc
https://pubmed.ncbi.nlm.nih.gov/19072095
https://pubmed.ncbi.nlm.nih.gov/19072095
Akademický článek
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Akademický článek
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Publikováno v:
The Journal of Organic Chemistry. 49:3503-3516
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91703e51051646db5601176b259b6484
https://doi.org/10.1021/jo00193a014
https://doi.org/10.1021/jo00193a014
Publikováno v:
Tetrahedron Letters. 26:1163-1166
An enantioselective synthesis of the tetrahydropyran “left-wing” ofthe ionophore X-14547A is described, wherein stereoselective 1,2-carbonyl additions and an oxapyronone-to-dihydropyran enolate Claisen rearrangement are key stereocontrol elements
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbc7f14af3336d6117e5212d82cff331
https://doi.org/10.1016/s0040-4039(00)98423-5
https://doi.org/10.1016/s0040-4039(00)98423-5
Publikováno v:
Tetrahedron Letters. 27:6295-6298
A synthesis of the “right-wing” equivalent 22 of the ionophore antibiotic indanomycin is described, wherein an unexpected retro hetero Diels-Alder/intramolecular Diels-Alder pathway gives the desired product of the planned Claisen [3,3]-shift.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b134a483441d58689f2c7b41709e159a
https://doi.org/10.1016/s0040-4039(00)87790-4
https://doi.org/10.1016/s0040-4039(00)87790-4