V
Venkata Ramana Doddi
Researcher at Central University of Karnataka
Publications - 23
Citations - 407
Venkata Ramana Doddi is an academic researcher from Central University of Karnataka. The author has contributed to research in topics: Ring-closing metathesis & Aryl. The author has an hindex of 11, co-authored 23 publications receiving 369 citations. Previous affiliations of Venkata Ramana Doddi include Indian Institute of Chemical Technology & University of Jammu.
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Reduction of amine N-oxides by diboron reagents.
TL;DR: The mechanism of the reductive process by (pinB)(2) has been probed by (1)H and (11)B NMR, and a sensitive nucleoside N-oxide has also been reduced efficiently.
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The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity
TL;DR: The dual role of the bicyclic amidine base 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) was demonstrated in a synthesis of terminal aryl- and styryl"-acetylenes from geminal dibromoalkenes, making it an attractive alternative to previous systems wherein required pyrophoric reagents and nonambient temperatures remain unsolved issues.
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Synthesis of hybrids of D-glucose and D-galactose with pyrrolidine-based iminosugars as glycosidase inhibitors
Venkata Ramana Doddi,Hari Prasad Kokatla,A. P. John Pal,Ranjan Kumar Basak,Yashwant D. Vankar +4 more
TL;DR: Sugar-iminosugar hybrid molecules made up of D-glucose and D-galactose with pyrrolidine-based iminosugars are synthesized from glycal epoxides and found to be moderate glycosidase inhibitors.
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Synthesis of fused pyran-carbahexopyranoses as glycosidase inhibitors.
TL;DR: Synthesis of polyhydroxylated oxabicyclo[4,4,0]decanes, which constitute a new family of annulated carbasugars, has been accomplished in a stereoselective manner by employing readily available 1,2-anhydro-3, 4,6-tri-O-benzyl-alpha-d-glycopyranoses.
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Synthesis of Pyrrolidine-Based Imino Sugars as Glycosidase Inhibitors
TL;DR: Two pyrrolidine-based imino sugars have been synthesized in an efficient manner, using regiospecific amination, ring closing metathesis, and diastereospecific dihydroxylations as key steps to be moderate inhibitors of glycosidases.