Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Petra Lindovska"'
Autor:
Justin Kim, Sean A. Newmister, Mohammad Movassaghi, Tyler J. Doyon, K. N. Houk, Vikram V. Shende, Petra Lindovska, Jacob N. Sanders, Yogan Khatri, Fengan Yu, David H. Sherman
Publikováno v:
J Am Chem Soc
The dimeric diketopiperazine (DKPs) alkaloids are a diverse family of natural products (NPs) whose unique structural architectures and biological activities have inspired the development of new synthetic methodology to access these molecules. However
Autor:
Petra Lindovska, Mohammad Movassaghi
Publikováno v:
Journal of the American Chemical Society. 139(48)
The enantioselective total synthesis of (−)-hodgkinsine, (−)-calycosidine, (−)-hodgkinsine B, (−)-quadrigemine C, and (−)-psycholeine through a diazene-directed assembly of cyclotryptamine fragments is described. Our synthetic strategy enab
Autor:
Dajian Zhu, Ri-Yuan Tang, Justin Kim, Peng Wang, Guoqiang Yang, Mohammad Movassaghi, Jin-Quan Yu, Petra Lindovska
Publikováno v:
Journal of the American Chemical Society. 136:10807-10813
meta-C-H olefination, arylation, and acetoxylation of indolines have been developed using nitrile-containing templates. The combination of a monoprotected amino acid ligand and the nitrile template attached at the indolinyl nitrogen via a sulfonamide
Publikováno v:
ChemInform. 47
We report a synthesis method for the construction of quaternary aryl phoshonium salts at ambient temperature. The regiospecific reaction involves the coupling of phosphines with aryl radicals derived from diaryliodonium salts under photoredox conditi
We report a synthesis method for the construction of quaternary aryl phoshonium salts at ambient temperature. The regiospecific reaction involves the coupling of phosphines with aryl radicals derived from diaryliodonium salts under photoredox conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d6da7e8506116e1fa363d0e1cda3a7e
http://eprints.nottingham.ac.uk/32151/
http://eprints.nottingham.ac.uk/32151/
Publikováno v:
Tetrahedron. 68:2899-2905
A metal-free catalytic method for the conversion of aromatic and aliphatic aldoximes to nitriles at room temperature using oxalyl chloride (1.2 equiv) in combination with 5 mol % of triphenylphosphine oxide is reported. Of the many potential pathways
Publikováno v:
Tetrahedron Letters. 52:6785-6787
A step-economical one-pot nucleophilic catalysis/thermal Claisen-rearrangement protocol for the direct synthesis of α-formyl-α-allylacetates from allylic alcohols and activated alkynes has been developed. The product α-formyl-α-allylacetates were
Autor:
Anupriya S. Kulkarni, Glen F. Deleavey, Petra Lindovska, Carlos González, Saúl Martínez-Montero, Nerea Martín-Pintado, Michael Thomson, Matthias Götte, Masad J. Damha
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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We report on the synthesis and conformational properties of 2′-deoxy-2′,4′-difluorouridine (2′,4′-diF-rU) and cytidine (2′,4′-diF-rC) nucleosides. NMR analysis and quantum mechanical calculations show that the strong stereoelectronic ef
Publikováno v:
ChemInform. 43
A metal-free and mild synthesis of the title compounds (II) and (IV) is developed by using inexpensive and readily available reagents.
Publikováno v:
ChemInform. 43
Thermal rearrangement of intermediately formed allyl vinyl ethers generates α-formyl-α-allylacetates which are isolated after reduction as alcohols or related O-protected enols.