(* = corresponding author)
38) Generation and application of alpha,alpha-diboryl radicals via thiyl radical catalyzed ring opening of vinyl cyclopropyl diborons: cis-Diastereoselective borylative cycloaddition with alkenes, H. Vyas, A. J. Gangani, A. Mini, S. Lin, J-M Chu, C. O. Agee, J. Gabriel, R. T. Williamson, Y. Zhang, A. Sharma,* Chem. Eur. J. 2023, DOI: 10.1002/chem.202303175
37) SERDs: A case study in targeted protein degradation; L. Wang, A. Sharma,* Chem. Soc. Rev. 2022, 51, 8149-8159.
(Invited article, Part of two themed collections “Modalities of induced proximity pharmacology: Degraders and Beyond” and "2022 emerging investigators")
36) Boron-promoted deprotonative conjugate addition: Geminal diborons as soft pronucleophiles and acyl anion equivalents; L. Wang, S. Lin, E. Santos, J. Pralat, K. Spotton, A. Sharma*, J. Org. Chem. 2022, 87, 9896-9906.
35) Acrylic boronate: A multifunctional C3 building block for catalytic synthesis of rare organoborons and chemoselective heterobifunctional ligations; S. Lin, L. Wang, A. Sharma*, Chemical Science, 2021, 12, 7924-7929.
34) α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and a-halo borons; L. Wang, S. Lin, Y. Zhu, D. Ferrante, T. Ishak, Y. Baba, A. Sharma*, Chem. Commun. 2021, 57, 4564-4567.
33) The quest for orally available selective estrogen receptor degraders (SERDs); L. Wang, A. Sharma*, ChemMedChem, 2020, 15, 2072-2097. (Selected as a Very Important Paper (VIP) by the reviewers)
32) A modular and concise approach to MIDA acylboronates via chemoselective oxidation of unsymmetrical geminal diborylalkanes: Unlocking access to a novel class of acylborons; S. Lin, L. Wang, N. Aminoleslami, Y. Lao, C. Yagel, A. Sharma*, Chemical Science, 2019, 10, 4684-4691.
31) Antagonists for constitutively active mutant estrogen receptors: Insights into the roles of antiestrogen-core and side-chain; A. Sharma,* W. Toy, V. S. Guillen, N. Sharma, J. Min, K. E. Carlson, C. G. Mayne, S. Lin, M. Sabio, G. Greene, B. S. Katzenellenbogen, S. Chandarlapaty, J. A. Katzenellenbogen, ACS Chem. Biol. 2018, 13, 3374-3384.
30) New class of selective estrogen receptor degraders (SERDs): Expanding the toolbox of PROTAC degrons; L. Wang, V.S. Guillen, N. Sharma, K. Flessa, J. Min, K. E. Carlson, W. Toy, S. Braqi, B. S. Katzenellenbogen, J. A. Katzenellenbogen, S. Chandarlapaty, A. Sharma,* ACS Med. Chem. Lett. 2018, 9, 803-808.
29) Recent advances in the synthesis and synthetic applications of 1,2,3-triazoles; S. Lin, A. Sharma,* Chem. Heterocycl. Compd. 2018, 54, 314-316.
28) Structurally novel antiestrogens elicit differential responses from constitutively active mutant estrogen receptors in breast cancer cells and tumors; Y. Zhao, M. J. Laws, V. S. Guillen, Y. Ziegler, J. Min, A. Sharma, S. H. Kim, D. Chu, B. H. Park, S. Oesterreich, C. Mao, D. J. Shapiro, K. W. Nettles, J. A. Katzenellenbogen, B. S. Katzenellenbogen, Cancer Res. 2017, 77, 5602-5613.
27) Adamantyl antiestrogens with novel side chains reveal a spectrum of activities in suppressing estrogen receptor mediated activities in breast cancer cells; J. Min, V. S. Guillen, A. Sharma, Y. Zhao, Y. Ziegler, P. Gong, C. G. Mayne, S. Srinivasan, S. H. Kim, K. E. Carlson, K. W. Nettles, B.S. Katzenellenbogen, J. A. Katzenellenbogen, J. Med. Chem. 2017, 60, 6321-6336
26) Exploring the structural compliancy versus specificity of the estrogen receptor using isomeric three-dimensional ligands; N. Sharma, K. Carlson, J. Nwachukwu, S. Srinivasan, A. Sharma, K. Nettles, J. A. Katzenellenbogen, ACS Chem. Biol. 2017, 12, 494–503.
25) Hydroxylated di- and tri-styrylbenzenes, a new class of antiplasmodial agents: discovery and mechanism of action; N. Sharma, D. Mohanakrishnan, A. Shard, A. Sharma, A. K. Sinha, D. A. Sahal, RSC Adv. 2016, 6, 49348-49357.
24) Insights into methyltransferase specificity and bioactivity of derivatives of the antibiotic plantazolicin; Y. Hao, P. M. Blair, A. Sharma, S. K. Nair, D. A. Mitchell, ACS Chem. Biol. 2015, 10, 1209-1216.
23) Triaryl-substituted schiff bases are high-affinity subtype-selective ligands for the estrogen receptor; Z.-Q. Liao, C. Dong, K. E. Carlson, S. Srinivasan, J. C. Nwachukwu, R. W. Chesnut, A. Sharma, K. W. Nettles, J.A. Katzenellenbogen, H.-B. Zhou, J. Med. Chem. 2014, 57, 3532-3545.
22) Synthesis of plantazolicin analogues enables dissection of ligand binding interactions of a highly selective methyltransferase; A. Sharma, P. M. Blair, D. A. Mitchell, Org. Lett. 2013, 15, 5076-5079.
21) Copper-catalyzed direct secondary and tertiary C-H alkylation of azoles through a novel Heteroarene-Amine-Aldehyde/Ketone coupling; D. Vachhani, A. Sharma, E. Van der Eycken, Angew. Chemie Int. Ed. 2013, 52, 2547-2550.
20) Direct heteroarylation of tautomerizable heterocycles into unsymmetrical and symmetrical biheterocycles via Pd/Cu-catalyzed phosphonium coupling; A. Sharma, D. Vachhani, E. Van der Eycken, Org. Lett. 2012, 14, 1854-1857.
19) Developments in direct C-H arylation of (hetero)arenes under microwave irradiation; A. Sharma, D. Vachhani, E. Van der Eycken, Chem. Eur. J. 2013, 19, 1158-1168.
18) Pd/Cu-catalyzed C-H arylation of 1,3,4-thiadiazoles with (hetero)aryl iodides, bromides and triflates; D. Vachhani, A. Sharma, E. Van der Eycken, J. Org. Chem. 2012, 77, 8768–8774.
17) A facile diversity-oriented synthesis of imidazo[1,2-a]pyrazinones via gold-catalyzed regioselective heteroannulation of propynylaminopyrazinones; D. Vachhani, S. G. Modha, A. Sharma, E. Van der Eycken, Tetrahedron, 2013, 69, 359-365.
16) Microwave-assisted synthesis of medium-sized heterocycles; A. Sharma, P. Appukkuttan; Chem. Commun. 2012, 48, 1623-1637.
15) Direct olefination of benzaldehydes into hydroxy functionalized oligo-(p-phenylenevinylene)s via Pd-catalyzed heterodomino Knoevenagel-decarboxylation-Heck sequence and its application for fluoride sensing p-conjugated units; A. Sharma, N. Sharma, R. Kumar, A. Shard and A. K. Sinha, Chem. Commun. 2010, 46, 3283-3285.
14) Water promoted cascade rearrangement approach towards α-aryl aldehydes from arylalkenes using N-halosuccinimides: An avenue for asymmetric oxidation using phase transfer cinchona organocatalysis; A. Sharma, N. Sharma, R. Kumar, U. Sharma and A. K. Sinha, Chem. Commun. 2009, 5299-5301.
13) Tandem allylic oxidation-condensation/esterification catalyzed by silica gel: An expeditious approach towards antimalarial diaryldienones and enones from natural methoxylated phenylpropenes; A. Sharma, N. Sharma, A. Shard, R. Kumar, D. Mohankrishnan, A. K. Sinha and D. Sahal, Org. Biomol. Chem. 2011, 9, 5211-5219.
12) Unique versatility of ionic liquids as clean decarboxylation catalyst cum solvent: A metal and quinoline-free paradigm towards synthesis of indoles, styrenes, stilbenes and arene derivatives under microwave irradiation in aqueous conditions; A. Sharma, R. Kumar, N. Sharma, V. Kumar and A. K. Sinha, Adv. Synth. Catal. 2008, 350, 2910-2920.
11) Stilbene−chalcone hybrids: design, synthesis, and evaluation as a new class of antimalarial scaffolds that trigger cell death through stage specific apoptosis; N. Sharma, D. Mohanakrishnan, A. Shard, A. Sharma, Saima, A. K. Sinha and D. Sahal, J. Med. Chem. 2012, 55, 297-311.
10) Pd-catalyzed orthogonal Knoevenagel/Perkin-decarboxylation-Heck/Suzuki sequences: Tandem transformation of benzaldehydes into hydroxy functionalized antidiabetic stilbene-cinnamoyl hybrids and unsymmetrical distyrylbenzenes; N. Sharma, A. Sharma, R. Kumar, A. Shard, Saima and A. K. Sinha, Chem. Eur. J. 2011, 17, 10350-10356.
9) One-pot two-step oxidative cleavage of 1,2-arylalkenes to aryl ketones instead of arylaldehydes in an aqueous medium: A complementary approach to ozonolysis; N. Sharma, A. Sharma, R. Kumar, A. Shard and A. K. Sinha, Eur. J. Org. Chem. 2010, 6025-6032.
8) Reinvestigation of structure–activity relationship of methoxylated chalcones as antimalarials: Synthesis and evaluation of 2,4,5-trimethoxy substituted patterns as lead candidates derived from abundantly available natural β-asarone; R. Kumar, D. Mohanakrishnan, A. Sharma, N. K. Kaushik, K. Kalia, A. K. Sinha and D. Sahal, Eur. J. Med. Chem. 2010, 45, 5292-5301.
7) Metal-free activation of H2O2 by synergic effect of ionic liquid and microwave: chemoselective oxidation of benzylic alcohols to carbonyls and unexpected formation of anthraquinone in aqueous condition ; R. Kumar, N. Sharma, N. Sharma, A. Sharma, and A. K. Sinha, Mol. Divers. 2011, 15, 687-695.
6) Green methodologies in synthesis and natural product chemistry of phenolic compounds, A. K. Sinha, N. Sharma, A. Shard, A. Sharma, R. Kumar and U. K. Sharma Ind. J. Chem.: Sec. B, 2009, 48, 1771-1779.
5) Neutral ionic liquid [hmim]Br as a green reagent and solvent for mild and efficient dehydration of benzyl alcohols into (E)-arylalkenes under microwave irradiation, R. Kumar, A. Sharma, N. Sharma, V. Kumar and A. K. Sinha, Eur. J. Org. Chem. 2008, 5577-5582.
4) Microwave assisted efficient extraction of different parts of Hippophae rhamnoides for the comparative evaluation of antioxidant activity and quantification of its phenolic constituents by RP-HPLC; U. Sharma, K. Sharma, N. Sharma, A. Sharma, H.P. Singh and A.K. Sinha, J. Ag. Food Chem. 2008, 56, 374-379.
3) An unusual, mild and convenient one pot two step access to (E)-Stilbenes from hydroxyl substituted benzaldehydes and phenyl acetic acids under microwave activation: Revelation of new facet on the classical perkin reaction; A. K. Sinha, V. Kumar, A. Sharma, and A. Sharma, Tetrahedron, 2007, 63, 11070–11077.
2) DDQ catalyzed benzylic acetoxylation of arylalkanes: A case of exquisitely controlled oxidation under sonochemical activation; V. Kumar, A. Sharma, M. Sharma, U. Sharma and A. K. Sinha, Tetrahedron, 2007, 63, 9718–9723.
1) Remarkable synergism in methylimidazole-promoted decarboxylation of substituted cinnamic acid derivatives in basic water medium under microwave irradiation: A clean synthesis of hydroxylated (E)-stilbenes; V. Kumar, A. Sharma, A. Sharma and A. K. Sinha, Tetrahedron, 2007, 63, 7640–7646.
Patents
4) INK4 tumor suppressor proteins mediate resistance to CDK4/6 kinase inhibitors; S. Chandarlapaty, L. Qing, N. Gray, B, Jiang, A. Sharma, A. Mini (PCT application filed, 2022)
3) Antiestrogen Compounds; A. Sharma, L. Wang, S. Lin (US 2021/0130320 A1)
2) One-pot multicomponent synthesis of some novel hydroxy stilbene derivatives with α, β-carbonyl conjugation under microwave irradiation; A. Sharma, A. K. Sinha, R. Kumar, N. Sharma, (US8716532B2)
1) Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues; A. K. Sinha, A. Sharma, R. Kumar and N. Sharma, (US8981152B2).
Books and Book Chapters
“Synthesis of medium-sized heterocycles under microwave irradiation” A. Sharma, E. Van der Eycken; Book chapter in textbook “Microwave Chemistry” Editors: G. Cravotto, D. Carnaroglio; 2017, Publisher: De Gruyter
38) Generation and application of alpha,alpha-diboryl radicals via thiyl radical catalyzed ring opening of vinyl cyclopropyl diborons: cis-Diastereoselective borylative cycloaddition with alkenes, H. Vyas, A. J. Gangani, A. Mini, S. Lin, J-M Chu, C. O. Agee, J. Gabriel, R. T. Williamson, Y. Zhang, A. Sharma,* Chem. Eur. J. 2023, DOI: 10.1002/chem.202303175
37) SERDs: A case study in targeted protein degradation; L. Wang, A. Sharma,* Chem. Soc. Rev. 2022, 51, 8149-8159.
(Invited article, Part of two themed collections “Modalities of induced proximity pharmacology: Degraders and Beyond” and "2022 emerging investigators")
36) Boron-promoted deprotonative conjugate addition: Geminal diborons as soft pronucleophiles and acyl anion equivalents; L. Wang, S. Lin, E. Santos, J. Pralat, K. Spotton, A. Sharma*, J. Org. Chem. 2022, 87, 9896-9906.
35) Acrylic boronate: A multifunctional C3 building block for catalytic synthesis of rare organoborons and chemoselective heterobifunctional ligations; S. Lin, L. Wang, A. Sharma*, Chemical Science, 2021, 12, 7924-7929.
34) α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and a-halo borons; L. Wang, S. Lin, Y. Zhu, D. Ferrante, T. Ishak, Y. Baba, A. Sharma*, Chem. Commun. 2021, 57, 4564-4567.
33) The quest for orally available selective estrogen receptor degraders (SERDs); L. Wang, A. Sharma*, ChemMedChem, 2020, 15, 2072-2097. (Selected as a Very Important Paper (VIP) by the reviewers)
32) A modular and concise approach to MIDA acylboronates via chemoselective oxidation of unsymmetrical geminal diborylalkanes: Unlocking access to a novel class of acylborons; S. Lin, L. Wang, N. Aminoleslami, Y. Lao, C. Yagel, A. Sharma*, Chemical Science, 2019, 10, 4684-4691.
31) Antagonists for constitutively active mutant estrogen receptors: Insights into the roles of antiestrogen-core and side-chain; A. Sharma,* W. Toy, V. S. Guillen, N. Sharma, J. Min, K. E. Carlson, C. G. Mayne, S. Lin, M. Sabio, G. Greene, B. S. Katzenellenbogen, S. Chandarlapaty, J. A. Katzenellenbogen, ACS Chem. Biol. 2018, 13, 3374-3384.
30) New class of selective estrogen receptor degraders (SERDs): Expanding the toolbox of PROTAC degrons; L. Wang, V.S. Guillen, N. Sharma, K. Flessa, J. Min, K. E. Carlson, W. Toy, S. Braqi, B. S. Katzenellenbogen, J. A. Katzenellenbogen, S. Chandarlapaty, A. Sharma,* ACS Med. Chem. Lett. 2018, 9, 803-808.
29) Recent advances in the synthesis and synthetic applications of 1,2,3-triazoles; S. Lin, A. Sharma,* Chem. Heterocycl. Compd. 2018, 54, 314-316.
28) Structurally novel antiestrogens elicit differential responses from constitutively active mutant estrogen receptors in breast cancer cells and tumors; Y. Zhao, M. J. Laws, V. S. Guillen, Y. Ziegler, J. Min, A. Sharma, S. H. Kim, D. Chu, B. H. Park, S. Oesterreich, C. Mao, D. J. Shapiro, K. W. Nettles, J. A. Katzenellenbogen, B. S. Katzenellenbogen, Cancer Res. 2017, 77, 5602-5613.
27) Adamantyl antiestrogens with novel side chains reveal a spectrum of activities in suppressing estrogen receptor mediated activities in breast cancer cells; J. Min, V. S. Guillen, A. Sharma, Y. Zhao, Y. Ziegler, P. Gong, C. G. Mayne, S. Srinivasan, S. H. Kim, K. E. Carlson, K. W. Nettles, B.S. Katzenellenbogen, J. A. Katzenellenbogen, J. Med. Chem. 2017, 60, 6321-6336
26) Exploring the structural compliancy versus specificity of the estrogen receptor using isomeric three-dimensional ligands; N. Sharma, K. Carlson, J. Nwachukwu, S. Srinivasan, A. Sharma, K. Nettles, J. A. Katzenellenbogen, ACS Chem. Biol. 2017, 12, 494–503.
25) Hydroxylated di- and tri-styrylbenzenes, a new class of antiplasmodial agents: discovery and mechanism of action; N. Sharma, D. Mohanakrishnan, A. Shard, A. Sharma, A. K. Sinha, D. A. Sahal, RSC Adv. 2016, 6, 49348-49357.
24) Insights into methyltransferase specificity and bioactivity of derivatives of the antibiotic plantazolicin; Y. Hao, P. M. Blair, A. Sharma, S. K. Nair, D. A. Mitchell, ACS Chem. Biol. 2015, 10, 1209-1216.
23) Triaryl-substituted schiff bases are high-affinity subtype-selective ligands for the estrogen receptor; Z.-Q. Liao, C. Dong, K. E. Carlson, S. Srinivasan, J. C. Nwachukwu, R. W. Chesnut, A. Sharma, K. W. Nettles, J.A. Katzenellenbogen, H.-B. Zhou, J. Med. Chem. 2014, 57, 3532-3545.
22) Synthesis of plantazolicin analogues enables dissection of ligand binding interactions of a highly selective methyltransferase; A. Sharma, P. M. Blair, D. A. Mitchell, Org. Lett. 2013, 15, 5076-5079.
21) Copper-catalyzed direct secondary and tertiary C-H alkylation of azoles through a novel Heteroarene-Amine-Aldehyde/Ketone coupling; D. Vachhani, A. Sharma, E. Van der Eycken, Angew. Chemie Int. Ed. 2013, 52, 2547-2550.
20) Direct heteroarylation of tautomerizable heterocycles into unsymmetrical and symmetrical biheterocycles via Pd/Cu-catalyzed phosphonium coupling; A. Sharma, D. Vachhani, E. Van der Eycken, Org. Lett. 2012, 14, 1854-1857.
19) Developments in direct C-H arylation of (hetero)arenes under microwave irradiation; A. Sharma, D. Vachhani, E. Van der Eycken, Chem. Eur. J. 2013, 19, 1158-1168.
18) Pd/Cu-catalyzed C-H arylation of 1,3,4-thiadiazoles with (hetero)aryl iodides, bromides and triflates; D. Vachhani, A. Sharma, E. Van der Eycken, J. Org. Chem. 2012, 77, 8768–8774.
17) A facile diversity-oriented synthesis of imidazo[1,2-a]pyrazinones via gold-catalyzed regioselective heteroannulation of propynylaminopyrazinones; D. Vachhani, S. G. Modha, A. Sharma, E. Van der Eycken, Tetrahedron, 2013, 69, 359-365.
16) Microwave-assisted synthesis of medium-sized heterocycles; A. Sharma, P. Appukkuttan; Chem. Commun. 2012, 48, 1623-1637.
15) Direct olefination of benzaldehydes into hydroxy functionalized oligo-(p-phenylenevinylene)s via Pd-catalyzed heterodomino Knoevenagel-decarboxylation-Heck sequence and its application for fluoride sensing p-conjugated units; A. Sharma, N. Sharma, R. Kumar, A. Shard and A. K. Sinha, Chem. Commun. 2010, 46, 3283-3285.
14) Water promoted cascade rearrangement approach towards α-aryl aldehydes from arylalkenes using N-halosuccinimides: An avenue for asymmetric oxidation using phase transfer cinchona organocatalysis; A. Sharma, N. Sharma, R. Kumar, U. Sharma and A. K. Sinha, Chem. Commun. 2009, 5299-5301.
13) Tandem allylic oxidation-condensation/esterification catalyzed by silica gel: An expeditious approach towards antimalarial diaryldienones and enones from natural methoxylated phenylpropenes; A. Sharma, N. Sharma, A. Shard, R. Kumar, D. Mohankrishnan, A. K. Sinha and D. Sahal, Org. Biomol. Chem. 2011, 9, 5211-5219.
12) Unique versatility of ionic liquids as clean decarboxylation catalyst cum solvent: A metal and quinoline-free paradigm towards synthesis of indoles, styrenes, stilbenes and arene derivatives under microwave irradiation in aqueous conditions; A. Sharma, R. Kumar, N. Sharma, V. Kumar and A. K. Sinha, Adv. Synth. Catal. 2008, 350, 2910-2920.
11) Stilbene−chalcone hybrids: design, synthesis, and evaluation as a new class of antimalarial scaffolds that trigger cell death through stage specific apoptosis; N. Sharma, D. Mohanakrishnan, A. Shard, A. Sharma, Saima, A. K. Sinha and D. Sahal, J. Med. Chem. 2012, 55, 297-311.
10) Pd-catalyzed orthogonal Knoevenagel/Perkin-decarboxylation-Heck/Suzuki sequences: Tandem transformation of benzaldehydes into hydroxy functionalized antidiabetic stilbene-cinnamoyl hybrids and unsymmetrical distyrylbenzenes; N. Sharma, A. Sharma, R. Kumar, A. Shard, Saima and A. K. Sinha, Chem. Eur. J. 2011, 17, 10350-10356.
9) One-pot two-step oxidative cleavage of 1,2-arylalkenes to aryl ketones instead of arylaldehydes in an aqueous medium: A complementary approach to ozonolysis; N. Sharma, A. Sharma, R. Kumar, A. Shard and A. K. Sinha, Eur. J. Org. Chem. 2010, 6025-6032.
8) Reinvestigation of structure–activity relationship of methoxylated chalcones as antimalarials: Synthesis and evaluation of 2,4,5-trimethoxy substituted patterns as lead candidates derived from abundantly available natural β-asarone; R. Kumar, D. Mohanakrishnan, A. Sharma, N. K. Kaushik, K. Kalia, A. K. Sinha and D. Sahal, Eur. J. Med. Chem. 2010, 45, 5292-5301.
7) Metal-free activation of H2O2 by synergic effect of ionic liquid and microwave: chemoselective oxidation of benzylic alcohols to carbonyls and unexpected formation of anthraquinone in aqueous condition ; R. Kumar, N. Sharma, N. Sharma, A. Sharma, and A. K. Sinha, Mol. Divers. 2011, 15, 687-695.
6) Green methodologies in synthesis and natural product chemistry of phenolic compounds, A. K. Sinha, N. Sharma, A. Shard, A. Sharma, R. Kumar and U. K. Sharma Ind. J. Chem.: Sec. B, 2009, 48, 1771-1779.
5) Neutral ionic liquid [hmim]Br as a green reagent and solvent for mild and efficient dehydration of benzyl alcohols into (E)-arylalkenes under microwave irradiation, R. Kumar, A. Sharma, N. Sharma, V. Kumar and A. K. Sinha, Eur. J. Org. Chem. 2008, 5577-5582.
4) Microwave assisted efficient extraction of different parts of Hippophae rhamnoides for the comparative evaluation of antioxidant activity and quantification of its phenolic constituents by RP-HPLC; U. Sharma, K. Sharma, N. Sharma, A. Sharma, H.P. Singh and A.K. Sinha, J. Ag. Food Chem. 2008, 56, 374-379.
3) An unusual, mild and convenient one pot two step access to (E)-Stilbenes from hydroxyl substituted benzaldehydes and phenyl acetic acids under microwave activation: Revelation of new facet on the classical perkin reaction; A. K. Sinha, V. Kumar, A. Sharma, and A. Sharma, Tetrahedron, 2007, 63, 11070–11077.
2) DDQ catalyzed benzylic acetoxylation of arylalkanes: A case of exquisitely controlled oxidation under sonochemical activation; V. Kumar, A. Sharma, M. Sharma, U. Sharma and A. K. Sinha, Tetrahedron, 2007, 63, 9718–9723.
1) Remarkable synergism in methylimidazole-promoted decarboxylation of substituted cinnamic acid derivatives in basic water medium under microwave irradiation: A clean synthesis of hydroxylated (E)-stilbenes; V. Kumar, A. Sharma, A. Sharma and A. K. Sinha, Tetrahedron, 2007, 63, 7640–7646.
Patents
4) INK4 tumor suppressor proteins mediate resistance to CDK4/6 kinase inhibitors; S. Chandarlapaty, L. Qing, N. Gray, B, Jiang, A. Sharma, A. Mini (PCT application filed, 2022)
3) Antiestrogen Compounds; A. Sharma, L. Wang, S. Lin (US 2021/0130320 A1)
2) One-pot multicomponent synthesis of some novel hydroxy stilbene derivatives with α, β-carbonyl conjugation under microwave irradiation; A. Sharma, A. K. Sinha, R. Kumar, N. Sharma, (US8716532B2)
1) Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues; A. K. Sinha, A. Sharma, R. Kumar and N. Sharma, (US8981152B2).
Books and Book Chapters
“Synthesis of medium-sized heterocycles under microwave irradiation” A. Sharma, E. Van der Eycken; Book chapter in textbook “Microwave Chemistry” Editors: G. Cravotto, D. Carnaroglio; 2017, Publisher: De Gruyter