46. Calcium(II) Catalyzed Cycloisomerization of cis-6-Hydroxy/(Acyloxy)hex-2-en-4-ynals to 2-Acyl- and 2-(Acyloxyalkenyl)furans. Soniya Gandhi and Beeraiah Baire. Chemistry Select, 2018, 3, 4490-4494.

45. Highly, regioselective electrophile induced cyclizations of 2-(prop-1-ynyl)benzamides. Bhavani Shankar Chinta, Harikrishna Sanapa, Kamala Prasad Vasikarla and Beeraiah Baire. Organic & Biomolecular Chemistry, 2018, 16, 2018,16, 3947-3951.

44. Synthetic Approach to seco-Tetracenomycin Natural Products Saccharothrixone A–C. Bhavani Shankar Chinta, Tapas Pal, Harikrishna Sanapa, Kamala Prasad Vasikarla and Beeraiah Baire. Tetrahedron Lett., 2018, 59, 1970-1973.

43. The Intercepted Meyer¬–Schuster Rearrangements in Organic Synthesis (review). Debayan Roy, Prabhakararao Tharra and Beeraiah Baire. Asian J. Org. Chem., 2018, 1015-1032.

42. An unprecedented (semi)Favorskii rearrangement. Evidence for the 2-acyloxycyclopropanones. Santu Sadhukhan and Beeraiah Baire. Org. Lett., 2018, 20, 1748-1751.

41. Regioselective Cyclization of (Indol-3-yl)pentyn-3-ols as an Approach to (Tetrahydro)carbazoles Prabhakararao Tharra and Beeraiah Baire. Org. Lett., 2018, 20, 1118-1121.

40. Total Synthesis of Selaginpulvilins A and C. Bhavani Shankar Chinta and Beeraiah Baire. Organic & Biomolecular Chemistry, 2018, 16, 262-265.

39. Lewis basicity of water for a selective monodehalogenation of α, α-dihaloketones to α-haloketones and mechanistic study. Santhu Sadhukhan and Beeraiah Baire, Advanced Synthesis and Catalysis, 2018, 360, 298-304.

38. Mechanistic Duality in Tertiary Amine Additions to Thermally Generated (HDDA) Benzynes. Sean P. Ross, Beeraiah Baire and Thomas R. Hoye. Org. Lett. 2017, 19, 5705-5708.

37. Ag(I) Catalyzed Cascade Approach to 2-(a-Hydroxyacyl)pyrroles. Soniya Gandhi and Beeraiah Baire. Chem. Select., 2017, 2, 3964-3968.

36. First Synthesis of [5-5-6-6] Tetracyclic Framework of Spiropreussione B. Bhavani Shankar Chinta and Beeraiah Baire. Eur. J. Org. Chem.,2017, 3457-3460. (Invited article)

35. Unconventional Reactivity of (z-enoate)Propargylic Alcohols in presence of Acids. Prabhakararao Tharra and Beeraiah Baire, Chemistry A European Journal, 2017, 23, 2014–2017.

34. Ag(I)-Catalyzed Cyclizative Hydration of Alkynes and Propargylic Alcohols. A Mild Approach to 2-Acylfuran Derivatives. Soniya Gandhi, Prabhakararao Tharra and Beeraiah Baire, Chemistry Select, 2017, 2, 1058-1062.

33. On the Distribution of Linear vs. Angular Naphthalenes in Aromatic Tetradehydro Diels-Alder Reaction: Effect of Linker Structure and Steric bulk. Bhavani Shankar Chinta and Beeraiah Baire. Eur. J. Org. Chem., 2017, 3381-3385.

32. Formal Total Synthesis of Selaginpulvilin D. Bhavani Shankar Chinta and Beeraiah Baire*, Org. Biomol. Chem., 2017, 15, 5908-5911. (Featured as cover page graphic)

31. Carbonyl Directed, Regioselective Hydration of Alkynes under Ag-Catalysis. Jampani Santhi and Beeraiah Baire*, Chem. Select. 2017, 2, 4338-4332.

30. A Coherent study on the Z-enoate assisted Meyer-Schuster rearrangement. Prabhakararao Tharra and Beeraiah Baire, Organic & Biomolecular Chemistry, 2017,15, 5579-5584.

29. An Expeditious Approach to α,α-Dihalo-α′-acetoxyketones from Propargylic acetates. Santu Sadhukhan and Beeraiah Baire, Chemistry Select, 2017, 2, 8500-8503.

28. Regioselective, Cascade [3+2] Annulation of b-Naphthols (Resorcinols) with Z-enoate Propargylic alcohols: A Novel entry into Complex Naphtho(benzo)furans. Prabhakararao Tharra and Beeraiah Baire, Chem. Comm., 2016, 52, 14290-14293.

27. Reactivity of indole-3-alkoxides in the absence of acids: Rapid synthesis of homo-bisindolylmethanes. Bhavani Shankar Chinta and Beeraiah Baire, Tetrahedron, 2016, 72, 8106-8116.

26. The dehydro Diels-Alder (DDA) reaction based approach to isofuranonaphthalenone, nodulones A-C and xestolactone A. Bhavani Shankar Chinta, Akshay Siraswar and Beeraiah Baire, Tetrahedron, 2017, 73, 4178-4185. (Invited Article)

25. Catalyst Free, Three-component Approach for Unsymmetrical Triarylmethanes (TRAMs). Bhavani Shankar Chinta and Beeraiah Baire, Tetrahedton Letters, 2016, 57, 5381-5384.

24. NIS promoted rapid access to indeno[1,2-c]pyrroles via [3+2] annulation of enamine-alkynes. Jampani Santhi and Beeraiah Baire, Adv. Synth. Catal. 2016. 358, 3817-3823.

23. A Systematic Study on Cadiot–Chodkiewicz Cross Coupling Reaction for Selective and Efficient Synthesis of hetero-diynes. Bhavani Shankar Chinta and Beeraiah Baire*, RSC Advances, 2016, 6, 54449-54455.

22. The Z-enoate, Assisted Meyer-Schuster Rearrangement Cascade: Unconventiona Synthesis of a-arylenone esters. Prabhakararao Tharra, and Beeraiah Baire, Chem Commun., 2016, 52, 12147-12150. (Featured as cover page graphic)

21. Mild Approach to 2-Acylfurans via Intercepted Meyer–Schuster Rearrangement of 6-Hydroxyhex-2-en-4-ynals. Prabhakararao Tharra and Beeraiah Baire, J. Org. Chem., 2015, 80, 8314-8328.

20. Stereoselective, Cascade Synthesis of trans-Enynones through Coupling-Isomerization Reaction Bhavani Shankar Chinta and Beeraiah Baire, J. Org. Chem., 2015, 80, 10208-10217.

19. Competition between classical and hexadehydro Diels-Alder (HDDA) reactions of HDDA triynes with furan. Quang L Nguyen, Beeraiah Baire and Thomas R Hoye, Tetrahedron Letters 2015, 56, 3265.

18. Tactics for probing aryne reactivity: mechanistic studies of silicon–oxygen bond cleavage during the trapping of (HDDA-generated) benzynes by silyl ethers. Thomas R Hoye, Beeraiah Baire, and Tao Wang. Chemical Science, 2014, 5, 545-550.

17. Ultra-High-Throughput Screening of Natural Product Extracts to Identify Proapoptotic Inhibitors of Bcl-2 Family Proteins. Christian A. Hassig et al. Susan G. Brown, Beeraiah Baire, Thomas R Hoye, Andrew R. Michel etc., Journal of biomolecular screening, 2014, 19, 1201-1211.

16. Rates of Hexadehydro Diels–Alder (HDDA) cyclizations: Impact of the Linker Structure. Brian P Woods, Beeraiah Baire, and Thomas R Hoye, Organic letters, 2014, 16, 4578.

15. Alkane desaturation via concerted dihydrogen transfer to benzyne. Dawen Niu, Patrick H. Willoughby, Brian P. Woods, Beeraiah Baire and Thomas R. Hoye, Nature, 2013, 501, 531-534.

14. Beeraiah Baire, Dawen Niu, Patrick H. Willoughby, Brian P. Woods and Thomas R. Hoye, Synthesis of complex benzenoids via the intermediate generation of o-benzynes through the hexadehydro-Diels-Alder reaction. Nat. Protoc., 2013, 8, 501-508.

13. Cycloaddition reactions of azide, furan, and pyrrole units with benzynes generated by the hexadehydro Diels-Alder (HDDA) reaction, Junhua Chen, Beeraiah Baire, and Thomas R. Hoye, Heterocycles, 2013, 88, 1191-1200.

12. The hexadehydro-Diels–Alder reaction. Thomas R. Hoye, Beeraiah Baire, Dawen Niu, Patrick H. Willoughby and Brian P. Woods, Nature, 2012, 490, 208-212.

11. Enantiospecific synthesis of the ABC-ring system of A-nor and abeo 4(3-2) tetra and pentacyclic triterpenes, A. Srikrishna, R. Ramesh Babu and B. Beeraiah, Tetrahedron, 2010, 66, 852-861.

10. Enantiospecific synthesis of the tricyclic core structure of lippifolianes, A. Srikrishna, R. Ramesh Babu and B. Beeraiah, Tetrahedron: Asymmetry, 2010, 21, 719-724.

9. Enantiospecific approach to the tricyclic core structure of tricyclo illicinone, ialibinones, and takaneones via ring-closing metathesis reaction, A. Srikrishna, B. Beeraiah and V. Gowri, Tetrahedron, 2009, 65, 2649-2654.

8. Enantioselective syntheses of cis, syn, cis- and cis, anti, cis-linear triquinanes, A. Srikrishna and B. Beeraiah, Tetrahedron: Asymmetry, 2008, 19, 884-890.

7. Enantioselective total synthesis of (+)-laurokamurene B, A. Srikrishna, B. Beeraiah and R. Ramesh Babu, Tetrahedron: Asymmetry, 2008, 19, 624-627.

6. Enantiospecific synthesis of the complete carbon framework of the diterpenes komarovispiranes, A. Srikrishna and B.          Beeraiah, Indian J. Chem., 2007, 46B, 1999-2003.

5. An enantiospecific synthesis of a komarovispirane, A. Srikrishna and B. Beeraiah,Tetrahedron: Asymmetry, 2007, 18, 2587-2597.

4. Synthesis of (±)-ar-macrocarpene, A. Srikrishna and B. Beeraiah, Synth. Commun., 2007, 37, 2855-2860.

3. Synthetic approaches to komarovispiranes. Enantiospecific synthesis of bicyclo[3.3.0]octanespiro- [3.1′]cyclohexanes, A. Srikrishna and B. Beeraiah, Tetrahedron Lett., 2007, 48, 2291-2294.

2. Chiral synthons from α-pinene: Enantioselective syntheses of bicyclo[3.3.0] and [3.2.1]octanones, A. Srikrishna, B. Beeraiah and G. Satyanarayana, Tetrahedron: Asymmetry, 2006, 17, 1544-1548.

1. First synthesis of (±)-tenuifolene and ar-tenuifolene, A. Srikrishna and B. Beeraiah, Indian J. Chem., 2005, 44B, 1641-1643.

  1. Cyclization methods. Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. Issued November 29, 2016 patent No. US 9,505,789.