Pavel Starkov
Overview
Explore the profile of Pavel Starkov including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
117
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Recent Articles
1.
Alam M, Ping K, Danilson M, Mikli V, Kaarik M, Leis J, et al.
ACS Appl Energy Mater
. 2024 May;
7(9):4076-4087.
PMID: 38756864
The use of precious metal electrocatalysts in clean electrochemical energy conversion and storage applications is widespread, but the sustainability of these materials, in terms of their availability and cost, is...
2.
Bhadoria R, Ping K, Lohk C, Jarving I, Starkov P
Chem Commun (Camb)
. 2020 Mar;
56(30):4216-4219.
PMID: 32181457
Various conjugation techniques are used to affect the intracellular delivery of bioactive small molecules. However, the ability to track changes in the phenotype when applying these tools remains poorly studied....
3.
Kasak L, Naks M, Eek P, Piirsoo A, Bhadoria R, Starkov P, et al.
Biochemistry
. 2018 Aug;
57(37):5456-5465.
PMID: 30096229
Serine/threonine protein kinase ULK3 is implicated in a variety of cellular processes, including autophagy, cell division, and execution of the Sonic hedgehog pathway. However, very little about how its biological...
4.
Starkov P, Moore J, Duquette D, Stoltz B, Marek I
J Am Chem Soc
. 2017 Jun;
139(28):9615-9620.
PMID: 28625056
We report a divergent and modular protocol for the preparation of acyclic molecular frameworks containing newly created quaternary carbon stereocenters. Central to this approach is a sequence composed of a...
5.
Lanigan R, Karaluka V, Sabatini M, Starkov P, Badland M, Boulton L, et al.
Chem Commun (Camb)
. 2016 Jun;
52(57):8846-9.
PMID: 27346362
A commercially available borate ester, B(OCH2CF3)3, can be used to achieve protecting-group free direct amidation of α-amino acids with a range of amines in cyclopentyl methyl ether. The method can...
6.
Starkov P, Jamison T, Marek I
Chemistry
. 2015 Feb;
21(14):5278-300.
PMID: 25641706
Among the numerous approaches and reagents employed for electrophilic amination, nitrenoids have long stayed out of the limelight. Here, we systematically review the discovery, structural features and chemical reactivity of...
7.
Lanigan R, Starkov P, Sheppard T
J Org Chem
. 2013 Apr;
78(9):4512-23.
PMID: 23586467
B(OCH2CF3)3, prepared from readily available B2O3 and 2,2,2-trifluoroethanol, is as an effective reagent for the direct amidation of a variety of carboxylic acids with a broad range of amines. In...
8.
Starkov P, Sheppard T
Org Biomol Chem
. 2011 Jan;
9(5):1320-3.
PMID: 21212879
Simple borates serve as effective promoters for amide bond formation with a variety of carboxylic acids and amines. With trimethyl or tris(2,2,2-trifluoroethyl) borate, amides are obtained in good to excellent...
9.
Korner C, Starkov P, Sheppard T
J Am Chem Soc
. 2010 Apr;
132(17):5968-9.
PMID: 20380452
A new method for enolate generation via the gold-catalyzed addition of boronic acids to alkynes is reported. The formation of boron enolates from readily accessible ortho-alkynylbenzeneboronic acids proceeds rapidly with...