K. N. Shavrin

417 total citations
53 papers, 325 citations indexed

About

K. N. Shavrin is a scholar working on Organic Chemistry, Pharmaceutical Science and Physical and Theoretical Chemistry. According to data from OpenAlex, K. N. Shavrin has authored 53 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Organic Chemistry, 8 papers in Pharmaceutical Science and 6 papers in Physical and Theoretical Chemistry. Recurrent topics in K. N. Shavrin's work include Cyclopropane Reaction Mechanisms (32 papers), Catalytic Alkyne Reactions (23 papers) and Catalytic Cross-Coupling Reactions (8 papers). K. N. Shavrin is often cited by papers focused on Cyclopropane Reaction Mechanisms (32 papers), Catalytic Alkyne Reactions (23 papers) and Catalytic Cross-Coupling Reactions (8 papers). K. N. Shavrin collaborates with scholars based in Russia and United States. K. N. Shavrin's co-authors include О. М. Нефедов, Mikhail P. Egorov, I. V. Krylova, С. Е. Боганов, Eugenii Ya. Misochko, Alexander V. Akimov, Денис В. Корчагин, V. I. Faustov, Yury V. Tomilov and E. V. Shulishov and has published in prestigious journals such as Journal of the American Chemical Society, Physical Chemistry Chemical Physics and The Journal of Physical Chemistry A.

In The Last Decade

K. N. Shavrin

50 papers receiving 323 citations

Peers

K. N. Shavrin

PTC

SPECT

З. В. Степанова Russia

Henry Giera Germany

M. Okada Japan

Denis N. Tomilin Russia

Kitae Kwon United States

Jean‐Luc Mieusset Austria

Rahul Kisan Kawade Taiwan

J. C. POMMELET France

Vasiliy G. Shtamburg Ukraine

A. A. Fainzil’berg Russia

З. В. Степанова Russia

K. N. Shavrin

334 ×1.1

50 ×0.8

62 ×1.6

PTC

45 ×2.5

SPECT

21 ×1.5

Citations per year, relative to K. N. Shavrin K. N. Shavrin (= 1×) peers З. В. Степанова

Countries citing papers authored by K. N. Shavrin

Since Specialization

Citations

This map shows the geographic impact of K. N. Shavrin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by K. N. Shavrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. N. Shavrin more than expected).

Fields of papers citing papers by K. N. Shavrin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K. N. Shavrin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by K. N. Shavrin. The network helps show where K. N. Shavrin may publish in the future.

Co-authorship network of co-authors of K. N. Shavrin

This figure shows the co-authorship network connecting the top 25 collaborators of K. N. Shavrin. A scholar is included among the top collaborators of K. N. Shavrin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with K. N. Shavrin. K. N. Shavrin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Shavrin, K. N., et al.. (2023). Electrophilic functionalization of N-substituted vicinal alkynyl(amino)cyclopropanes via selective lithiation. Russian Chemical Bulletin. 72(8). 1781–1790. 2 indexed citations

Shavrin, K. N., et al.. (2019). Alkylthio(4-methylpent-3-en-1-ynyl)carbenes: generation by the photolysis of 5-alkylthioethynyl-3,3-dimethyl-3H-pyrazoles and reactions with alkenes. Mendeleev Communications. 29(2). 140–142. 6 indexed citations

Shavrin, K. N., et al.. (2019). New synthesis of 3,3-disubstituted piperidin-2-ones from esters and 1-(3-halopropyl)-2,5-dimethylpyrroles. Russian Chemical Bulletin. 68(11). 2108–2113. 1 indexed citations

Shavrin, K. N., et al.. (2019). Infrared-Spectroscopic Study of (4-Methylpent-3-en-1-ynyl)methylthiocarbene, Its Photochemical Transformations, and Reactions in an Argon Matrix. The Journal of Physical Chemistry A. 123(42). 9175–9184. 7 indexed citations

Shavrin, K. N., et al.. (2018). New selective cyclizations of alk-4-ynals with primary amines and azoles:one-pot synthesis of 2-azolylpyrrolidines and 3-iminocyclopentenes. Mendeleev Communications. 28(2). 123–125. 2 indexed citations

Shavrin, K. N., et al.. (2015). One-pot synthesis of 1-arylmethylidene-1,2,3,3a-tetrahydro-5H-pyrrolo[1,2-a]-[3,1]benzoxazines and 1-arylmethylidene-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]-quinazolines from 5-arylalk-4-ynals and o-aminobenzylic alcohol/amine. Mendeleev Communications. 25(5). 329–331. 6 indexed citations

Shavrin, K. N., et al.. (2014). A new synthesis of bicyclic N,O- and N,S-enaminals by the anionic cyclization of alk-4-ynals with amino alcohols and amino thiols. Russian Chemical Bulletin. 63(2). 409–415. 6 indexed citations

Shavrin, K. N., et al.. (2013). Selective Reduction and Dehydrogenation of 6-Benzylideneoctahydropyrrolo[1,2-a]Pyrimidines and 5-Benzylidenehexahydropyrrolo[1,2-a]Imidazoles as New Approaches to N-(ω-Aminoalkyl)Pyrrolidines and Bicyclic Amidines. Mendeleev Communications. 23(1). 31–33. 5 indexed citations

Shavrin, K. N., et al.. (2013). Synthesis of 6-(arylmethylidene)octahydropyrrolo[1,2-a]pyrimidines and 5-(arylmethylidene)hexahydropyrrolo[1,2-a]imidazoles by the interaction of alk-4-ynals with a,?-diaminoalkanes in DMSO in the presence of KOH. Mendeleev Communications. 23(3). 140–141. 10 indexed citations

10.

Misochko, Eugenii Ya., et al.. (2012). Matrix isolation ESR spectroscopy and quantum chemical calculations on 5-methylhexa-1,2,4-triene-1,3-diyl, a highly delocalized triplet “hybrid” carbene. Physical Chemistry Chemical Physics. 14(6). 2032–2032. 11 indexed citations

11.

Shavrin, K. N., et al.. (2010). Synthesis of 5-methylidenehexahydropyrrolo[l,2-a]imidazoles and 6-methylideneoctahydropyrrolo[l,2-a]pyrimidines by the reaction of 1-alkynyl-1-chlorocyclopropanes with lithium derivatives of 1,2- and 1,3-diaminoalkanes. Russian Chemical Bulletin. 59(7). 1451–1458. 14 indexed citations

12.

Shavrin, K. N., et al.. (2008). Unusual reactions of 1-(alk-1-ynyl)-1-chlorocyclopropanes with lithium monoalkylamides. Mendeleev Communications. 18(1). 16–17. 9 indexed citations

13.

Shavrin, K. N., et al.. (2008). Reaction of 1-(alk-1-ynyl)-1-halocyclopropanes with alcohols and phenol in KOH/DMSO as a method for the synthesis of 2-alkoxy-1-alkynyl- and 1-alkynyl-2-phenoxycyclopropanes. Russian Chemical Bulletin. 57(10). 2117–2124. 8 indexed citations

14.

Shavrin, K. N., et al.. (2002). Alk-1-ynyl(3-pyridyl)- and alk-1-ynyl(2-thienyl)carbenes as the first example of (alk-1-ynyl)carbenes with hetaryl substituents at carbenic centres. Mendeleev Communications. 12(6). 224–225. 6 indexed citations

15.

Tomilov, Yury V., et al.. (1998). Reaction of diazoalkanes with unsaturated compounds. Russian Chemical Bulletin. 47(11). 2208–2212. 1 indexed citations

16.

Shavrin, K. N., et al.. (1997). A new, general route to 1-chloro-1-ethynylcyclopropanes via chloro(trimethylsilylethynyl)carbene. Mendeleev Communications. 7(6). 218–219. 1 indexed citations

17.

Shavrin, K. N., et al.. (1997). A new general method for the generation of (alk-1-ynyl)halocarbenes by base solvolysis of 3-substituted 1,1,1,3-tetrahalopropanes. Mendeleev Communications. 7(4). 144–145. 7 indexed citations

18.

Shavrin, K. N., et al.. (1993). Chlorovinylidenecarbene: generation from 3,3-dichloropropyne by interaction with potassium hydroxide under phase-transfer catalysis conditions and reactions with alkenes. Russian Chemical Bulletin. 42(7). 1185–1187. 1 indexed citations

19.

Shavrin, K. N., et al.. (1986). (2-Fukyl)- and (2-theinyl)chlorocarbenes ? New carbenes with heterocyclic substituents. Russian Chemical Bulletin. 35(10). 2180–2184. 1 indexed citations

20.

Shavrin, K. N., et al.. (1984). (2-Furyl)- and (2-thienyl) chlorocarbenes - New carbenes with heterocyclic substituents. Russian Chemical Bulletin. 33(11). 2424–2424.

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