A.R.A.S. Deshmukh

1.2k total citations
74 papers, 889 citations indexed

About

A.R.A.S. Deshmukh is a scholar working on Organic Chemistry, Molecular Biology and Cancer Research. According to data from OpenAlex, A.R.A.S. Deshmukh has authored 74 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Organic Chemistry, 15 papers in Molecular Biology and 11 papers in Cancer Research. Recurrent topics in A.R.A.S. Deshmukh's work include Synthesis of β-Lactam Compounds (39 papers), Synthesis and Catalytic Reactions (28 papers) and Asymmetric Synthesis and Catalysis (14 papers). A.R.A.S. Deshmukh is often cited by papers focused on Synthesis of β-Lactam Compounds (39 papers), Synthesis and Catalytic Reactions (28 papers) and Asymmetric Synthesis and Catalysis (14 papers). A.R.A.S. Deshmukh collaborates with scholars based in India and United States. A.R.A.S. Deshmukh's co-authors include B. M. Bhawal, Vedavati G. Puranik, Bidhan A. Shinkre, A. Jayanthi, Vaidyanathan Srirajan, Benjamin N. Bhawal, Muthusamy Jayaraman, S. RAJAPPA, Edward R. Biehl and V. S. JOSHI and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Tetrahedron Letters.

In The Last Decade

A.R.A.S. Deshmukh

71 papers receiving 835 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
A.R.A.S. Deshmukh India 16 832 185 158 91 47 74 889
B. M. Bhawal India 17 618 0.7× 170 0.9× 125 0.8× 58 0.6× 44 0.9× 57 691
В. А. Глушков Russia 11 586 0.7× 127 0.7× 64 0.4× 70 0.8× 27 0.6× 92 636
Michael J. Totleben United States 12 570 0.7× 157 0.8× 40 0.3× 77 0.8× 17 0.4× 15 743
Plato Α. Magriotis United States 16 715 0.9× 173 0.9× 37 0.2× 144 1.6× 38 0.8× 28 810
Indrani Banik United States 14 952 1.1× 109 0.6× 114 0.7× 101 1.1× 49 1.0× 22 1.0k
Guangzhong Wu United States 18 957 1.2× 80 0.4× 54 0.3× 139 1.5× 21 0.4× 19 1.0k
Yasuyuki Kita Japan 17 810 1.0× 99 0.5× 55 0.3× 66 0.7× 17 0.4× 34 884
Yoshizumi Yasui Japan 16 997 1.2× 156 0.8× 68 0.4× 145 1.6× 10 0.2× 36 1.0k
Carolina Fernández-Rivas Spain 9 643 0.8× 113 0.6× 137 0.9× 101 1.1× 21 0.4× 9 807
Cristina Aragoncillo Spain 23 1.8k 2.2× 197 1.1× 96 0.6× 203 2.2× 18 0.4× 50 1.9k

Countries citing papers authored by A.R.A.S. Deshmukh

Since Specialization
Citations

This map shows the geographic impact of A.R.A.S. Deshmukh'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 A.R.A.S. Deshmukh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.R.A.S. Deshmukh more than expected).

Fields of papers citing papers by A.R.A.S. Deshmukh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.R.A.S. Deshmukh. 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 A.R.A.S. Deshmukh. The network helps show where A.R.A.S. Deshmukh may publish in the future.

Co-authorship network of co-authors of A.R.A.S. Deshmukh

This figure shows the co-authorship network connecting the top 25 collaborators of A.R.A.S. Deshmukh. A scholar is included among the top collaborators of A.R.A.S. Deshmukh 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 A.R.A.S. Deshmukh. A.R.A.S. Deshmukh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Puranik, Vedavati G., et al.. (2007). Stereoselective synthesis of spiro-β-lactams using d-(+)-glucose derived chiral pool: remarkable influence of the torquoelectronic effect. Tetrahedron. 63(37). 9179–9187. 12 indexed citations
2.
Puranik, Vedavati G., et al.. (2007). Asymmetric synthesis of β-lactams by [2+2] cycloaddition using 1,4:3,6-dianhydro-d-glucitol (isosorbide) derived chiral pools. Tetrahedron. 63(16). 3380–3388. 23 indexed citations
3.
Bhawal, B. M., et al.. (2004). Microwave assisted phase transfer catalysis: an efficient solvent free method for the synthesis of cyclopropane derivatives. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 43(2). 420–422. 4 indexed citations
4.
Deshmukh, A.R.A.S., et al.. (2004). Azetidin-2-ones, Synthon for Biologically Important Compounds †. Current Medicinal Chemistry. 11(14). 1889–1920. 164 indexed citations
5.
Deshmukh, A.R.A.S., et al.. (2004). Synthesis of Polycyclic β-Lactams fromd-Glucose Derived Chiral Template via Substrate-Controlled Radical Cyclization. Synthesis. 2965–2974. 4 indexed citations
6.
Deshmukh, A.R.A.S., et al.. (2004). One-pot preparation of dialkylcarbamoyl azides from tertiary amines using triphosgene and sodium azide. Tetrahedron Letters. 45(35). 6571–6573. 10 indexed citations
8.
Puranik, Vedavati G., et al.. (2003). Asymmetric synthesis of azetidin-2-ones by [2+2] cycloaddition using chiral imines derived from d-(+)-glucose. Tetrahedron. 59(13). 2309–2316. 26 indexed citations
9.
Deshmukh, A.R.A.S., et al.. (2002). Synthesis of azetidin-2-one via in situ generated acid chlorides using hexachloroacetone-triethylphosphite. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 41(4). 856–857.
10.
Bhawal, B. M., et al.. (2002). A mild and efficient method for the preparation of acyl azides from carboxylic acids using triphosgene. Tetrahedron Letters. 43(7). 1345–1346. 26 indexed citations
11.
Bhawal, B. M., et al.. (2002). Triphosgene: a versatile reagent for the synthesis of azetidin-2-ones. Tetrahedron. 58(11). 2215–2225. 42 indexed citations
12.
Deshmukh, A.R.A.S., et al.. (2000). An efficient synthesis of enantiomerically pure 3-hydroxy-β-lactams via zinc induced removal of a chiral auxiliary. Tetrahedron Asymmetry. 11(7). 1477–1485. 15 indexed citations
13.
Srirajan, Vaidyanathan, Vedavati G. Puranik, A.R.A.S. Deshmukh, & B. M. Bhawal. (1996). An efficient use of Oppolzer sultam for Diastereospecific Synthesis of cis-β-Lactams. Tetrahedron. 52(15). 5579–5584. 15 indexed citations
14.
Deshmukh, A.R.A.S., et al.. (1995). Conformational preferences of α-functionalised keten-S,N-acetals: Potential role of SO and SS interactions in solution. Tetrahedron. 51(5). 1437–1448. 21 indexed citations
15.
Bhawal, B. M., et al.. (1995). Use of Zeolite Catalysts for Efficient Synthesis of Benzoxazoles via Beckmann Rearrangement. Synthetic Communications. 25(21). 3315–3321. 25 indexed citations
16.
Jayaraman, Muthusamy, A.R.A.S. Deshmukh, & B. M. Bhawal. (1994). Efficient Asymmetric Synthesis of cis-4-Formyl .beta.-Lactams from L-(+)-Tartaric Acid. The Journal of Organic Chemistry. 59(4). 932–934. 34 indexed citations
17.
18.
Jayaraman, Muthusamy, A.R.A.S. Deshmukh, & B. M. Bhawal. (1992). Remote Stereocontrol in Ketene-Imine Cycloaddition: An Efficient Asymmetric Synthesis ofcis-β-Lactams. Synlett. 1992(9). 749–750. 14 indexed citations
19.
Deshmukh, A.R.A.S., et al.. (1989). AN IMPROVED PROCEDURE FOR THE PREPARATION OF 1,1,1-TRICHLORO-4-METHYL-3-PENTEN-2-YL DIAZOACETATE. Organic Preparations and Procedures International. 21(4). 509–511.
20.
MITRA, R. B., et al.. (1982). A New Route to 3-Phenoxybenzyl cis (±) 2,2-Dimethyl-3-(2-Phenyl-2-Chlorovinyl) Cyclopropanecarboxylate. Synthetic Communications. 12(13). 1063–1070. 3 indexed citations

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