2-Azabicyclo [2.2. 1] hept-5-en-3-one: chemical profile of a versatile synthetic building block and its impact on the development of therapeutics

R Singh, R Vince - Chemical Reviews, 2012 - ACS Publications
Replacement of the furanosyl oxygen with a methylene unit in the ribose sugar in
nucleosides 1 and nucleotides 2 prompted the rise of a new nucleoside class with very …

Synthesis of Bicyclonucleosides Having a C− C Bridge

J Lebreton, JM Escudier, L Arzel, C Len - Chemical reviews, 2010 - ACS Publications
Typical nucleosides are initially obtained from the nucleic acids, DNA and RNA, by
enzymatic hydrolysis, and they are of great biological importance in metabolic pathways. 1 …

Nucleosides having bicyclic sugar moiety

Z Hong, H An - US Patent 6,833,361, 2004 - Google Patents
BACKGROUND Nucleoside and nucleotide analogs have long been used as
pharmaceutical ingredients against a variety of viruses and cancers. Currently, a number of …

Nucleosides having bicyclic sugar moiety

G Wang - US Patent 6,403,566, 2002 - Google Patents
BACKGROUND Nucleoside and nucleotide analogs have long been used as
pharmaceutical ingredients against a variety of viruses and cancers. Currently, a number of …

Diastereo-and enantioselective synthesis of orthogonally protected 2, 4-diaminocyclopentanecarboxylates: A flip from β-amino-to β, γ-diaminocarboxylates

L Kiss, E Forró, R Sillanpää, F Fülöp - The Journal of Organic …, 2007 - ACS Publications
Conformationally restricted, orthogonally protected 2, 4-diaminocarboxylates with a
cyclopentane skeleton were efficiently synthesized from β-lactam 6, the syntheses involving …

Conformationally locked nucleosides. Synthesis and stereochemical assignments of 2′-C, 4′-C-bridged bicyclonucleosides

G Wang, JL Girardet, E Gunic - Tetrahedron, 1999 - Elsevier
1-α-O-Methyl-3-O, 5-O-TIPDS-arabinose was converted, in multiple steps, to 2, 6-dioxa-
bicyclo [3, 2, 1] octane derivatives, which were condensed with silylated nucleoside bases to …

The synthesis of single enantiomers of meromycolic acids from mycobacterial wax esters

R Juma'a, MS Baird, E Roberts, DE Minnikin - Tetrahedron, 2006 - Elsevier
Three stereoisomers of a wax ester meromycolate have been prepared starting from
mannitol. A detailed comparison of their NMR spectra with those reported for a homologous …

Synthesis and conformational analysis of new cyclobutane-fused nucleosides

R Alibés, A Alvárez-Larena, P De March… - Organic …, 2006 - ACS Publications
A stereselective synthesis of 3-oxabicyclo [3.2. 0] heptane nucleoside analogues, which
were designed as conformational mimics of the anti-HIV agents 2 ', 3 '-didehydro-2 ', 3 ' …

The synthesis of (11R, 12S)-lactobacillic acid and its enantiomer

GD Coxon, JR Al-Dulayymi, MS Baird, S Knobl… - Tetrahedron …, 2003 - Elsevier
(11R, 12S)-Lactobacillic acid has been prepared from 2, 3-O-isopropylidene-d-
glyceraldehyde, in a sequence involving asymmetric cyclopropanation, and from cis …

Enantiomeric Syntheses of Conformationally Restricted d- and l-2',3'-Dideoxy-2',3'-endo-methylene Nucleosides from Carbohydrate Chiral Templates

BK Chun, S Olgen, JH Hong, MG Newton… - The Journal of Organic …, 2000 - ACS Publications
d-and l-2 ', 3 '-dideoxy-2 ', 3 '-endo-methylene nucleosides were synthesized as potential
antiviral agents. The key intermediates 5-O-tert-butyldiphenylsilyl-d-and l-2, 3-dideoxy-2, 3 …