نتایج جستجو برای: 2h pyrans

تعداد نتایج: 11400  

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2001
F Gómez-Garibay M D Arciniega C L Céspedes J Taboada J S Calderón

The aerial parts of Tephrosia carrollii afforded two chromene chalcones. Their structures and stereochemistry were established by spectroscopic methods. The structure of oaxacacin was revised and confirmed by X-ray diffraction. In this paper, we describe the isolation of the chalcone known as "oaxacacin" and the new chalcone named epoxyobovatachalcone. The compound der. oaxacacin was found to b...

Journal: :Organic & biomolecular chemistry 2016
Reece Jacques Ritashree Pal Nicholas A Parker Claire E Sear Peter W Smith Aubert Ribaucourt David M Hodgson

In the past two decades, alkene metathesis has risen in prominence to become a significant synthetic strategy for alkene formation. Many total syntheses of natural products have used this transformation. We review the use, from 2003 to 2015, of ring-closing alkene metathesis (RCM) for the generation of dihydrofurans or -pyrans in natural product synthesis. The strategies used to assemble the RC...

Journal: :The Journal of general virology 1999
D Genovese S Catone M E Farah A Gambacorta L Fiore

Poliovirus type 2 Sabin mutants were selected for drug resistance and dependence by plating on HeLa cell monolayers in the presence of 3(2H)-isoflavene, a compound related to dichloroflavan, which prevents the shut-off of host translation and poliovirus RNA and protein synthesis. The drug-resistant mutants grew equally well in the presence and in the absence of the drug, while the drug-dependen...

2009
Ding Ye Kuan Zhang Hua-feng Chen Shu-fan Yin Ying Li

The title compound, C(21)H(24)O(11), crystallizes exclusively as the β-anomer. The substituent of the protected sugar at position C-3 is in the axial position, while all other groups are in equatorial positions. The pyran-oside ring adopts a stable chair conformation.

2009
Christoph Böttcher Gehad Zeyat Saleh A Ahmed Elisabeth Irran Thorben Cordes Cord Elsner Wolfgang Zinth Karola Rueck-Braun

Photochromic pyrans for applications in material and life sciences were synthesized via palladium-mediated cyanation, carbonylation and Sonogashira cross-coupling starting from bromo-substituted naphthopyran 1 and benzopyrans 2a/b. A novel photoswitchable benzopyran-based omega-amino acid 6 for Fmoc-based solid-phase peptide synthesis is presented. The photochromic behaviour of the 3-cyano-subs...

Journal: :Organic & biomolecular chemistry 2009
Volker Belting Norbert Krause

Depending on the substitution pattern and the solvent, the gold-catalyzed cyclization of alk-4-yn-1-ones affords different oxygen heterocycles under mild reaction conditions. Alkynones with one substituent at C-3 undergo a 5-exo-dig cycloisomerization to substituted furans , whereas a 6-endo-dig cyclization to 4H-pyrans is observed with substrates bearing two substituents at C-3. In alcoholic s...

2010
S. Thenmozhi A. SubbiahPandi S. Kathiravan R. Raghunathan

In the title compound, C(25)H(25)NO(4), the pyrrolidine ring exhibits an envelope conformation and the tetra-hydro-pyran ring exhibits a half-chair conformation. The crystal structure is stabilized by inter-molecular C-H⋯π inter-actions.

Journal: :Journal of the American Chemical Society 2006
Benjamin D Sherry Lisa Maus Brian Ngo Laforteza F Dean Toste

A trinuclear gold(I)-oxo complex, [(Ph3PAu)3O]BF4, serves as the catalyst for the stereocontrolled synthesis of 2-hydroxy-3,6-dihydropyrans from propargyl vinyl ethers. Importantly, the rearrangement proceeds with excellent diastereoselectivity, and the rearrangement of chiral nonracemic propargyl vinyl ethers proceeds with excellent chirality transfer to furnish enantioenriched pyrans. Additio...

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