Yerri Jagadeesh - Concepedia

Author

Yerri Jagadeesh

Indian Institute of Chemical Technology

Also Known As

Jagadeesh, Yerri, Y. Jagadeesh, Yerri Jagadeesh

Publications

141

Citations

H-Index

Concepts

All Affiliations

Indian Institute of Chemical Technology

About

Yerri Jagadeesh is an author at Indian Institute of Chemical Technology specializing in organic chemistry, biomolecular engineering, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	4	4	72
2	Biomolecular Engineering	4	4	72
3	Biochemistry	3	3	51
4	Natural Sciences	2	2	53
5	Medicine	1	1	30

Yerri Jagadeesh

Publications

127

Citations

H-Index

Page 1

	Year	Citations
Synthesis of 1,2-<i>cis</i>-Homoiminosugars Derived from GlcNAc and GalNAc Exploiting a β-Amino Alcohol Skeletal Rearrangement Yves Blériot, Nicolas Auberger, Yerri Jagadeesh, Organic Letters Bioorganic ChemistryGlycobiologyMolecular BiologyPeptide ScienceCarbohydrate-protein Interaction	2014	30
DDQ-Promoted Benzylic/Allylic sp<sup>3</sup> C–H Activation for the Stereoselective Intramolecular C–N Bond Formation: Applications to the Total Synthesis of (−)-Codonopsinine, (+)-5-<i>epi</i>-Codonopsinine, (+)-Radicamine B, and (−)-Codonopsinol Lingamurthy Macha, Yerri Jagadeesh, Katakam Ramakrishna, The Journal of Organic Chemistry -Radicamine BAmide-tethered Benzylic/allylic SystemEngineeringTotal SynthesisOrganic Chemistry	2016	28
Total synthesis of (−)-codonopsinol and (+)-2-epi codonopsinol via acid catalyzed amido cyclisation Yerri Jagadeesh, J. Santhosh Reddy, B. Venkateswara Rao, Tetrahedron Novel OrganocatalystsBioorganic ChemistryEngineeringNatural SciencesDiversity-oriented Synthesis	2009	23
Total synthesis of radicamine B and 5-epi-radicamine B Yerri Jagadeesh, B. Venkateswara Rao Tetrahedron Letters Diversity-oriented SynthesisTotal SynthesisOrganic ChemistryPharmacologyNatural Product Synthesis	2011	13
Chiron approach to (−)-deoxocuscohygrine Yerri Jagadeesh, Kotha Kapu Sridhar Reddy, B. Venkateswara Rao Tetrahedron Asymmetry Structure ElucidationOrganic ChemistryChiron ApproachChemistryDeoxygenation	2011	12
The synthesis of (1S,8aS)-1-hydroxyindolizidine using a stereoselective Grignard addition to an N-benzyl-3-deoxy sugar imine derived from D-Glucose Yerri Jagadeesh, B. Chandrasekhar, B. Venkateswara Rao Tetrahedron Asymmetry EngineeringN-benzyl-3-deoxy Sugar ImineBiochemistryStereoselective Grignard AdditionOrganic Chemistry	2010	11
A common synthetic approach for seven and eight-membered polyhydroxylated iminocyclitols Yerri Jagadeesh, Katakam Ramakrishna, B. Venkateswara Rao Tetrahedron Asymmetry Diversity Oriented SynthesisEngineeringHeterocyclicBiochemistryCommon Synthetic Approach	2012	10

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