B. M. Bhawal

962 total citations
57 papers, 691 citations indexed

About

B. M. Bhawal is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, B. M. Bhawal has authored 57 papers receiving a total of 691 indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 10 papers in Molecular Biology and 7 papers in Oncology. Recurrent topics in B. M. Bhawal's work include Synthesis of β-Lactam Compounds (29 papers), Synthesis and Catalytic Reactions (18 papers) and Asymmetric Synthesis and Catalysis (14 papers). B. M. Bhawal is often cited by papers focused on Synthesis of β-Lactam Compounds (29 papers), Synthesis and Catalytic Reactions (18 papers) and Asymmetric Synthesis and Catalysis (14 papers). B. M. Bhawal collaborates with scholars based in India, United States and Japan. B. M. Bhawal's co-authors include A.R.A.S. Deshmukh, Vedavati G. Puranik, Muthusamy Jayaraman, Vaidyanathan Srirajan, S. RAJAPPA, Subhash P. Khanapure, Edward R. Biehl, T. Indrasena Reddy, Mukund K. Gurjar and Hanumant B. Borate and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Tetrahedron Letters.

In The Last Decade

B. M. Bhawal

52 papers receiving 645 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. M. Bhawal India 17 618 170 125 58 44 57 691
A.R.A.S. Deshmukh India 16 832 1.3× 185 1.1× 158 1.3× 91 1.6× 47 1.1× 74 889
Michael J. Totleben United States 12 570 0.9× 157 0.9× 40 0.3× 77 1.3× 17 0.4× 15 743
Plato Α. Magriotis United States 16 715 1.2× 173 1.0× 37 0.3× 144 2.5× 38 0.9× 28 810
Yasuyuki Kita Japan 17 810 1.3× 99 0.6× 55 0.4× 66 1.1× 17 0.4× 34 884
В. А. Глушков Russia 11 586 0.9× 127 0.7× 64 0.5× 70 1.2× 27 0.6× 92 636
Eloı́sa Martı́n-Zamora Spain 18 693 1.1× 216 1.3× 29 0.2× 131 2.3× 20 0.5× 31 785
Vishnumaya Bisai India 15 926 1.5× 193 1.1× 43 0.3× 181 3.1× 51 1.2× 28 985
Masatoshi Murakata Japan 14 514 0.8× 131 0.8× 27 0.2× 97 1.7× 17 0.4× 31 586
Carolina Fernández-Rivas Spain 9 643 1.0× 113 0.7× 137 1.1× 101 1.7× 21 0.5× 9 807
Vikram C. Purohit United States 11 636 1.0× 130 0.8× 21 0.2× 98 1.7× 20 0.5× 15 739

Countries citing papers authored by B. M. Bhawal

Since Specialization
Citations

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

Fields of papers citing papers by B. M. Bhawal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B. M. Bhawal. 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 B. M. Bhawal. The network helps show where B. M. Bhawal may publish in the future.

Co-authorship network of co-authors of B. M. Bhawal

This figure shows the co-authorship network connecting the top 25 collaborators of B. M. Bhawal. A scholar is included among the top collaborators of B. M. Bhawal 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 B. M. Bhawal. B. M. Bhawal 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.
Bhawal, B. M., et al.. (2010). A Novel Method for Resolution of Amlodipine. Organic Process Research & Development. 14(3). 640–643. 39 indexed citations
2.
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
3.
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
4.
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
5.
Bhusare, Sudhakar R., et al.. (2003). New Synthesis of 1-Aryl-4-(4-hydroxy-3,5-diiodo-α-methylbenzylidene)-2-phenylimidazol-5-ones. Chemistry of Heterocyclic Compounds. 39(6). 726–728. 2 indexed citations
6.
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.
7.
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
8.
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
9.
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
10.
Srirajan, Vaidyanathan, et al.. (1997). Novel Protective Group in β-Lactam Chemistry: 3-Phenoxy-4-phenyl-N-[α-(phenylthio)benzyl]azetidin-2-one. Acta Crystallographica Section C Crystal Structure Communications. 53(3). 358–360. 1 indexed citations
11.
Srirajan, Vaidyanathan, et al.. (1997). Synthesis of N1-unsubstituted β-lactams: Introducing N1-(1′-thiophenyl)benzyl as an N-protecting group. Tetrahedron Letters. 38(24). 4281–4284. 11 indexed citations
12.
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
13.
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
14.
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
15.
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
16.
Reddy, T. Indrasena, B. M. Bhawal, & S. RAJAPPA. (1992). A facile general method for the preparation of s-methyl thiolcarbamates using zeolite catalysts. Tetrahedron Letters. 33(20). 2857–2860. 13 indexed citations
17.
Bhawal, B. M., Subhash P. Khanapure, & Edward R. Biehl. (1991). Transesterification of Methyl Arylacetates with Lithium Alkoxides. Synthesis. 1991(2). 112–114. 7 indexed citations
18.
Bhawal, B. M., et al.. (1991). Synthesis and X-ray structure of cis-4b,9b-diphenyl-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-5,10-dione. Journal of the Chemical Society Chemical Communications. 743–743.
19.
Khanapure, Subhash P., B. M. Bhawal, & Edward R. Biehl. (1990). Use of N-lithiated ethyl anthranilates as 1,4-dipole equivalents in 1,4-dipolearyne cycloaddition: A novel approach to the synthesis of acridones. Tetrahedron Letters. 31(20). 2869–2872. 6 indexed citations
20.
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.

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