Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ruja Shrestha"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 12, Pp m1830-m1830 (2011)
In the title compound, [Pd(C7H7O2S)Cl(C44H32P2)]·3CH2Cl2·H2O, the geometry around the metal atom is distorted square planar, with a twist angle between the P—Pd—P and S—Pd—Cl planes of 28.11 (2)°. The two Pd—P bond lengths differ by abou
Externí odkaz:
https://doaj.org/article/b1f09c047bb0439a9def87f6c305e556
Publikováno v:
Journal of Advanced Academic Research. 10:63-74
Newborn care is a set of comprehensive recommendations designed by World Health Organization (WHO) to improve health of the Newborn through intervention before conception, during pregnancy, soon after birth and in postnatal period. It includes Thermo
Publikováno v:
Organic Letters
Conjugate addition of organometallic reagents to enones to form silyl enol ether products is a versatile method to difunctionalize activated olefins, but the organometallic reagents required can be limiting. The reductive cross-electrophile coupling
Publikováno v:
Journal of the American Chemical Society. 135:751-762
An alternative method to copper-catalyzed conjugate addition followed by enolate silylation for the synthesis of β-disubstituted silyl enol ether products (R(1)(R(2))HCCH═C(OSiR(4)(3))R(3)) is presented. This method uses haloarenes instead of nucl
Publikováno v:
Zhang, Jing; Shrestha, Ruja; Hartwig, John F.; & Zhao, Pinjing. (2016). A decarboxylative approach for regioselective hydroarylation of alkynes. Nature Chemistry, 8(12). Lawrence Berkeley National Laboratory: Lawrence Berkeley National Laboratory. Retrieved from: http://www.escholarship.org/uc/item/4xq057pv
Regioselective activation of aromatic C-H bonds is a long-standing challenge for arene functionalization reactions such as the hydroarylation of alkynes. One possible solution is to employ a removable directing group that activates one of several aro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8229ee79f6db2a2a6d687f965cae614
http://www.escholarship.org/uc/item/4xq057pv
http://www.escholarship.org/uc/item/4xq057pv
Publikováno v:
ChemInform. 46
The title reaction proceeds with high regio- and stereoselectivity to provide (E)-β-aryl alkenoates as major products.
Publikováno v:
Tetrahedron letters. 56(23)
The direct, regioselective, and stereoselective arylation of activated alkynes with aryl iodides using a nickel catalyst and manganese reductant is described. The reaction conditions are mild (40 °C in MeOH, no acid or base) and an intermediate orga
Autor:
Brandon E. Johnson, Nijee Sharma, Tulaza Vaidya, Sara Herrera, Ruja Shrestha, Katrina Brandis, Shubhik K. DebBurman
Publikováno v:
Journal of Molecular Neuroscience. 28:161-178
Parkinson's disease (PD) is a common neurodegenerative disorder that results from the selective loss of midbrain dopaminergic neurons. Misfolding and aggregation of the protein alpha-synuclein, oxidative damage, and proteasomal impairment are all hyp
Publikováno v:
Journal of the American Chemical Society. 135(23)
We report the Pd-catalyzed amination of arenes to form N-aryl phthalimides with regioselectivity controlled predominantly by steric effects. Mono-, di-, and trisubstituted arenes lacking a directing group undergo amination reactions with moderate to
Autor:
Daniel J. Weix, Ruja Shrestha
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4d66c11e4a272550b484ca978d4c3de
https://doi.org/10.1002/047084289x.rn01502
https://doi.org/10.1002/047084289x.rn01502