The 3, 4-dioxygenated 5-hydroxy-4-aryl-quinolin-2 (1 H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products

SO Simonetti, EL Larghi, TS Kaufman - Natural product reports, 2016 - pubs.rsc.org
Covering: up to April 2016 Aspergillus and Penicillium are fungal species known to produce
a high diversity of secondary metabolites, many of them endowed with interesting bioactivity …

A review of methods to synthesise 4′-substituted nucleosides

M Betson, N Allanson, P Wainwright - Organic & Biomolecular …, 2014 - pubs.rsc.org
Modified nucleosides have received a great deal of attention from the scientific community,
either for use as therapeutic agents, diagnostic tools, or as molecular probes. Perhaps the …

Enantioselective, intermolecular [2+ 2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (−)-pinolinone

F Mayr, C Wiegand, T Bach - Chemical Communications, 2014 - pubs.rsc.org
Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone:
total synthesis of (−)-pinolinone - Chemical Communications (RSC Publishing) DOI:10.1039/C3CC49469A …

The Chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2009

JW Herndon - Coordination chemistry reviews, 2011 - Elsevier
This is a review of papers published in the year 2009 that focus on the synthesis, reactivity,
or properties of compounds containing a carbon-transition metal double or triple bond.

Synthesis of glaucogenin D, a structurally unique disecopregnane steroid with potential antiviral activity

J Gui, H Tian, W Tian - Organic letters, 2013 - ACS Publications
The first chemical synthesis of glaucogenin D, a 13, 14: 14, 15-disecopregnane steroid with
potential antiviral activity, has been accomplished in 12 steps from a hirundigenin-type …

Synthesis of 4 '-Methyl and 4 '-Cyano Carbocyclic 2 ', 3 '-Didehydro Nucleoside Analogues via 1, 4-Addition to Substituted Cyclopentenones

LS Hegedus, J Cross - The Journal of Organic Chemistry, 2004 - ACS Publications
Carbocyclic 4 '-methyl and 4 '-cyano nucleoside analogues were synthesized using the
Michael reaction to introduce the 4 '-substituent and Pd-catalyzed allylic substitution to …

Synthesis of 4'α-C phenyl-branched carbocyclic nucleoside using ring-closing metathesis

JH Hong, OH Ko - Bulletin of the Korean Chemical Society, 2003 - koreascience.kr
An efficient synthetic route for preparing novel $4'{\alpha} $-C phenyl branched carbocyclic
nucleoside is described. The installation of phenyl group at the $4'$-position of carbocyclic …

A practical synthetic route to 4′-alkylaristeromycin derivatives: 4′-methylaristeromycin

X Yin, SW Schneller - Tetrahedron letters, 2006 - Elsevier
(−)-(1S, 4R)-4-Hydroxy-2-cyclopenten-1-yl acetate provided a convenient entry point for a 16-
step chiral preparation of 4′-methylaristeromycin. This procedure is adaptable to a number …

A Ferrier-Type Allylic Rearrangement of 3′-Deoxy-3′, 4′-didehydronucleosides Mediated by DMF Dimethyl Acetal: Direct Access to 4′-Alkoxy-2′, 3′-didehydro …

M Petrová, M Buděšínský, E Zborníková… - Organic …, 2011 - ACS Publications
A Ferrier-Type Allylic Rearrangement of 3′-Deoxy-3′,4′-didehydronucleosides Mediated
by DMF Dimethyl Acetal: Direct Access to 4′-Alkoxy-2′,3′-didehydro-2′,3′-dideoxynucleosides …

Photoinduced Reactions of Metal Carbenes in Organic Synthesis

LS Hegedus - Metal Carbenes in Organic Synthesis: -/-, 2004 - Springer
The photoinduced reactions of metal carbene complexes, particularly Group 6 Fischer
carbenes, are comprehensively presented in this chapter with a complete listing of …