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Your search keyword '"Trusar D. Bagul"' showing total 3 results
Start Over Author "Trusar D. Bagul" Topic biochemistry
3 results on '"Trusar D. Bagul"'

1. An expeditious synthesis of epibatidine and analogues

Author

Trusar D. Bagul, G. Lakshmaiah, and Ganesh Pandey

Subjects
Bicyclic molecule, Stereochemistry, Chemistry, Organic Chemistry, Azomethine ylide, Biochemistry, Cycloaddition, chemistry.chemical_compound, Epibatidine, Drug Discovery, Pyridine, medicine, Stereoselectivity, medicine.drug
Abstract

An efficient synthesis of Epibatidine and its analogues via [3+2] cycloaddition of non-stabilised azomethine ylide and substituted 6-chloro-3-vinyl pyridine.

Published
1994

2. Total Synthesis of Spirotryprostatin B via Asymmetric Nitroolefination

Author

Takeo Kawabata, Trusar D. Bagul, Kaoru Fuji, and Gingipalli Lakshmaiah

Subjects
Indoles, Pyrrolidines, Stereochemistry, Aspergillus fumigatus, Organic Chemistry, Total synthesis, Stereoisomerism, Biochemistry, Growth Inhibitors, Piperazines, chemistry.chemical_compound, chemistry, Spiro Compounds, Physical and Theoretical Chemistry, Spirotryprostatin B
Abstract

[reaction: see text] A total synthesis of spirotryprostatin B was accomplished via asymmetric nitroolefination as a key step.

Published
2001

3. [3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x-Azatricyclo[m.n.0.0a,b]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide

Author

Ganesh Pandey, Trusar D. Bagul, and and Akhila K. Sahoo

Subjects
chemistry.chemical_classification, Trimethylsilyl, Stereochemistry, Organic Chemistry, Azomethine ylide, Biochemistry, Medicinal chemistry, Cycloaddition, chemistry.chemical_compound, chemistry, Ylide, Intramolecular force, Physical and Theoretical Chemistry, Cyclic amines
Abstract

Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the intramolecular [3 + 2] dipolar cycloaddition of nonstabilized cyclic azomethine ylides. The ylide is generated by the sequential double desilylation of N-alkyl α,α‘-bis(trimethylsilyl)cyclic amines using Ag(I)F as a one-electron oxidant.

Published
2000

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