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of 30
pro vyhledávání: '"Goreti, Rajendar"'
Publikováno v:
In Tetrahedron 15 January 2024 150
Autor:
Mathew, George, Silva, Saulo L. L., Jain, Anil, Mohan, Arya, Adroja, D. T., Sakai, V. G., Tomy, C. V., Banerjee, Alok, Goreti, Rajendar, N., Aswathi V., Singh, Ranjit, Jaiswal-Nagar, D.
Publikováno v:
Phys. Rev. Research 2, 043329 (2020)
Quantum entanglement is a quantum mechanical phenomenon where the quantum state of a many-body system with many degrees of freedom cannot be described independently of the state of each body with a given degree of freedom, no matter how far apart in
Externí odkaz:
http://arxiv.org/abs/2010.15747
Akademický článek
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Publikováno v:
Synthesis.
A concise and stereoselective synthesis of a key fragment C3-C22 unit of tartrolons D and E is demonstrated. Three crucial fragments are combined to form the 20-carbon chain, which contains four stereogenic centers in the monomeric unit of both natur
Publikováno v:
Organic letters. 24(33)
A new class of highly regio- and stereoselective intramolecular rearrangements of glycidol acetals to produce alkoxylated 1,3-dioxolane/1,3-dioxane is demonstrated. Selective Lewis acid activation of acetal generates an oxocarbenium ion that initiate
Autor:
Goreti Rajendar, Ranganayakulu Sunnapu
Publikováno v:
European Journal of Organic Chemistry. 2021:1637-1642
Autor:
Reyno R S, Goreti Rajendar, Ranganayakulu Sunnapu, Aleena Thomas, Saikumar Naik Banoth, Navyasree Venugopal
Publikováno v:
The Journal of Organic Chemistry. 85:4103-4113
The first stereoselective total synthesis of (-)-(2S,4R)-3'-methoxy citreochlorol and (-)-(2S,4S)-3'-methoxy citreochlorol is demonstrated. A proline-based imidazolidinone was synthesized and used as chiral auxiliary for asymmetric acetate aldol reac
Publikováno v:
Organicbiomolecular chemistry. 20(2)
Modified reaction conditions for improved
Autor:
Ranganayakulu, Sunnapu, Saikumar Naik, Banoth, Reyno, R S, Aleena, Thomas, Navyasree, Venugopal, Goreti, Rajendar
Publikováno v:
The Journal of organic chemistry. 85(6)
The first stereoselective total synthesis of (-)-(2
Publikováno v:
Organic letters. 22(3)
An efficient method for the preparation of β-amino-α,β-unsaturated carbonyl compounds is demonstrated. Bench-stable sodium 3-oxo-enolates were prepared from carbonyl compounds, and reacted with amines in the presence of an acid and a desiccant. DF