2 article(s) from Stark, Christian B W
Putative structures of geraniol 1a (R = H) or 1b (R = H) (in 1924), their expected dihydroxylation ...
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Correlation between the substrate double bond geometry and relative stereochemistry of the correspo...
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Mechanisms and classification for the metal-mediated oxidative cyclizations to form 2,5-disubstitut...
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Synthesis of (+)-anhydro-D-glucitol and (+)-D-chitaric acid using an OsO4-mediated oxidative cycliz...
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Total synthesis of neodysiherbaine A via a Ru(VIII)- and an Os(VI)-catalyzed oxidative cyclization,...
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Formal synthesis of ionomycin by Kocienski and co-workers.
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Total synthesis of amphidinolide F by Fürstner and co-workers.
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Brown`s and Donohoe`s oxidative cyclization approach to cis-solamin A.
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Total synthesis of cis-solamin A using a Ru(VIII)-catalyzed oxidative cyclization and enzymatic des...
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Donohoe´s double oxidative cyclization approach to cis-sylvaticin.
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Permanganate-mediated approach to cis-sylvaticin by Brown and co-workers.
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Total synthesis of membranacin using a KMnO4-mediated oxidative cyclization.
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Total synthesis of membrarollin and its analogue 21,22-diepi-membrarollin.
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Total synthesis of rollidecin C and D using a late stage Re(VII)-catalyzed oxidative polycyclizatio...
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Co(II)-catalyzed oxidative cyclization in the total synthesis of asimilobin and gigantetrocin A.
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Mn(VII)-catalyzed oxidative cyclization of a 1,5-diene in the synthesis of trans-(+)-linalool oxide....
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Re(VII)-catalyzed oxidative cyclization in the total synthesis of teurilene.
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Total synthesis of (+)-eurylene via Re(VII)- and Cr(VI)-mediated oxidative cyclizations.
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Synthesis of cis- and trans-THF Rings of eurylene via Mn(VII)-mediated oxidative cyclizations.
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Cr(VI)-catalyzed oxidative cyclization in the total synthesis of venustatriol by Corey et al.
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Ru(VIII)-catalyzed oxidative cyclization of a 1,5-diene in the synthesis and evaluation of its ster...
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Ru(VII)-catalyzed oxidative cyclization of a 5,6-dihydroxy alkene in the synthesis of the core stru...
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Beilstein J. Org. Chem. 2016, 12, 2104–2123, doi:10.3762/bjoc.12.200
Known heronapyrroles A–C and nitropyrrolins A–E.
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Plausible biosynthesis of heronapyrroles A–D.
Synthesis of heronapyrrole D.
Beilstein J. Org. Chem. 2014, 10, 1228–1232, doi:10.3762/bjoc.10.121
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