Publications

An efficient one-step chemoselective reduction of alkyl ketones over aryl ketones in ß-diketones using LiHMDS and lithium aluminium hydride.

S. Veera Swamy, K. Indrasena Reddy, R. Venkat Ragavan, K. Tirumal Reddy, Satyanarayana Yennam, A. Jayashree.

Tetrahedron Letters., 53, 2012, 4651-4653.

An efficient method for the preparation of mono a-aryl derivatives of diethyl cyanoacetate using ethyl-1-imidazole carbamate (ElmC).

Manoranjan Behera, R. Venkatragavan, M. Sambaiah, Balaiah Erugu, J. Rama Krishna Reddy, K. Mukkanti, Satyanarayana Yennam.

Tetrahedron Letters., 53, (2012), 1060-1062.

Pd-catalyzed amination of 6-halo-2-cyclopropyl-3-(pyridyl-3-ylmethyl) quinazolin-4(3H)-one

Ramesh Garlapati, Narender Pottabathini, Venkateshwarlu Gurram, Avinash B. Chaudhary, Venkata Rao Chunduri, Balaram Patro

Tetrahedron Letters 2012, 53, 5162–5166.

Synthesis of novel isoxazole-benzoquinone hybrids via 1,3-dipolar cycloaddition reaction as key step

P. Ravi Kumar, Manoranjan Behera, K. Raghavulu, A. Jaya Shree, Satyanarayana

Tetrahedron Letters 2012, 53, 4108–4113

Synthesis and Cytotoxicity Testing of New Amido-Substituted Triazolopyrrolo[2,1-c][1,4]benzodiazepine (PBDT) Derivatives

Kumaraswamy Sorra, Chi-Fen Chang, Srinivas Pusuluri, Khagga Mukkanti, Min-Chiau Laiu, Bo-Ying Bao, Chia-Hao Su and Ta-Hsien Chuang

Molecules 2012, 17, 8762-8772

C–C Cross-Coupling Reactions of O6-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/O6-Deprotection Procedure

Venkateshwarlu Gurram, Narender Pottabathini*, Ramesh Garlapati, Avinash B. Chaudhary, Balaram Patro, and Mahesh K. Lakshman*

Chemistry-An Asian Journal, 2012, 7(8), 1853-1861

Enantiospecific first total synthesis of 7a(S)-p-hydroxyphenopyrrozin

Yugandhar Kothapalli, Ravi Kumar Puthukanoori, Srinivasa Rao Alapati

Tetrahedron Letters 2012; 53, 1891–1893

Palladium catalyzed synthesis of quinazolino [1,4] benzodiazepine alkaloids and analogues

Kumaraswamy Sorra, Srinivas Pusuluri and K. Mukkanti

Tetrahedron 2012; 68, 2001-2006

Flow Chemistry vs. Batch Processes

Pharmacokinetic Strategies in CNS Drug Discovery

An efficient one-step chemoselective reduction of alkyl ketones over aryl ketones in ß-diketones using LiHMDS and lithium aluminium hydride.

An efficient method for the preparation of mono a-aryl derivatives of diethyl cyanoacetate using ethyl-1-imidazole carbamate (ElmC).

Pd-catalyzed amination of 6-halo-2-cyclopropyl-3-(pyridyl-3-ylmethyl) quinazolin-4(3H)-one

Synthesis of novel isoxazole-benzoquinone hybrids via 1,3-dipolar cycloaddition reaction as key step

Synthesis and Cytotoxicity Testing of New Amido-Substituted Triazolopyrrolo[2,1-c][1,4]benzodiazepine (PBDT) Derivatives

C–C Cross-Coupling Reactions of O6-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/O6-Deprotection Procedure

Enantiospecific first total synthesis of 7a(S)-p-hydroxyphenopyrrozin

Palladium catalyzed synthesis of quinazolino [1,4] benzodiazepine alkaloids and analogues

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Pharmacokinetic Strategies in CNS Drug Discovery

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Publications

An efficient one-step chemoselective reduction of alkyl ketones over aryl ketones in ß-diketones using LiHMDS and lithium aluminium hydride.

An efficient method for the preparation of mono a-aryl derivatives of diethyl cyanoacetate using ethyl-1-imidazole carbamate (ElmC).

Pd-catalyzed amination of 6-halo-2-cyclopropyl-3-(pyridyl-3-ylmethyl) quinazolin-4(3H)-one

Synthesis of novel isoxazole-benzoquinone hybrids via 1,3-dipolar cycloaddition reaction as key step

Synthesis and Cytotoxicity Testing of New Amido-Substituted Triazolopyrrolo[2,1-c][1,4]benzodiazepine (PBDT) Derivatives

C–C Cross-Coupling Reactions of O6-Alkyl-2-Haloinosine Derivatives and a One-Pot Cross-Coupling/O6-Deprotection Procedure

Enantiospecific first total synthesis of 7a(S)-p-hydroxyphenopyrrozin

Palladium catalyzed synthesis of quinazolino [1,4] benzodiazepine alkaloids and analogues