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Raju Jannapu Reddy
Observed names:
Jannapu Reddy, Raju,
Raju Jannapu Reddy,
Raju Jannapu Reddy,
Reddy, Raju Jannapu
Institution:
Osmania University
Observed institutions:
Central University of Karnataka,
National Taiwan Normal University,
Kyoto Pharmaceutical University,
University of Hyderabad,
Thieme Medical Publishers (Germany),
University of Birmingham,
Osmania University
show all 7
ORCID:
0000-0002-0667-6787
Observed ORCID:
0000-0002-0667-6787
OpenAlex ID:
A5005860038
The Baylis–Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry
2007
·
Deevi Basavaiah
, Kalapala Venkateswara Rao
, et al.
·
Chemical Society Reviews
·
477
Synthesis and applications of sodium sulfinates (RSO 2 Na): a powerful building block for the synthesis of organosulfur compounds
2021
·
Raju Jannapu Reddy
, Arram Haritha Kumari
·
RSC Advances
·
215
PDF
Alkynyl Thioethers in Gold‐Catalyzed Annulations To Form Oxazoles
2017
·
Raju Jannapu Reddy
, Matthew P. Ball‐Jones
, et al.
·
Angewandte Chemie International Edition
·
115
PDF
Recent advances in the synthesis and applications of β-keto sulfones: new prospects for the synthesis of β-keto thiosulfones
2021
·
Raju Jannapu Reddy
, Arram Haritha Kumari
, et al.
·
Organic & Biomolecular Chemistry
·
85
Pyrrolidinyl–Camphor Derivatives as a New Class of Organocatalyst for Direct Asymmetric Michael Addition of Aldehydes and Ketones to β‐Nitroalkenes
2010
·
Ying‐Fang Ting
, Chihliang Chang
, et al.
·
Chemistry - A European Journal
·
78
Efficient and Flexible Synthesis of Highly Functionalised 4‐Aminooxazoles by a Gold‐Catalysed Intermolecular Formal [3+2] Dipolar Cycloaddition
2016
·
Andrew D. Gillie
, Raju Jannapu Reddy
, et al.
·
Advanced Synthesis & Catalysis
·
74
PDF
Highly diastereo- and enantioselective direct aldol reactions promoted by water-compatible organocatalysts bearing a pyrrolidinyl-camphor structural scaffold
2009
·
Zheng-Hao Tzeng
, Hung-Yao Chen
, et al.
·
Tetrahedron
·
64
Pyrrolidine‐Camphor Derivative as an Organocatalyst for Asymmetic Michael Additions of α,α‐Disubstituted Aldehydes to β‐Nitroalkenes: Construction of Quaternary Carbon‐Bearing Aldehydes under Solvent‐Free Conditions
2009
·
Chihliang Chang
, Ssu‐Hsien Li
, et al.
·
Advanced Synthesis & Catalysis
·
61
Novel Prolinamide–Camphor‐Containing Organocatalysts for Direct Asymmetric Michael Addition of Unmodified Aldehydes to Nitroalkenes
2009
·
Raju Jannapu Reddy
, Hsuan‐Hao Kuan
, et al.
·
Chemistry - A European Journal
·
59
Unprecedented Reactivity of β‐Iodovinyl Sulfones: An Efficient Synthesis of β‐Keto Sulfones and β‐Keto Thiosulfones
2019
·
Raju Jannapu Reddy
, Jangam Jagadesh Kumar
, et al.
·
European Journal of Organic Chemistry
·
50
Highly Efficient Organocatalytic Kinetic Resolution of Activated Nitroallylic Acetates with Aldehydes via Conjugate Addition−Elimination
2011
·
Raju Jannapu Reddy
, Kwunmin Chen
·
Organic Letters
·
48
Cs2CO3‐Mediated Vicinal Thiosulfonylation of 1,1‐Dibromo‐1‐Alkenes with Thiosulfonates: An Expedient Synthesis of (E)‐1,2‐Thiosulfonylethenes
2019
·
Raju Jannapu Reddy
, Arram Haritha Kumari
, et al.
·
Advanced Synthesis & Catalysis
·
47
Simple, Facile, and One-Pot Conversion of the Baylis−Hillman Adducts into Functionalized 1,2,3,4-Tetrahydroacridines and Cyclopenta[b]quinolines
2004
·
Deevi Basavaiah
, Jamjanam Srivardhana Rao
, et al.
·
The Journal of Organic Chemistry
·
47
Applications of Baylis–Hillman adducts: a simple, convenient, and one-pot synthesis of 3-benzoylquinolines
2005
·
Deevi Basavaiah
, Raju Jannapu Reddy
, et al.
·
Tetrahedron Letters
·
46
Pd‐Catalyzed Annulation of β‐Iodovinyl Sulfones with 2‐Halophenols: A General Route for the Synthesis of 3‐Sulfonyl Benzofuran Derivatives
2020
·
Raju Jannapu Reddy
, Jangam Jagadesh Kumar
, et al.
·
Advanced Synthesis & Catalysis
·
41
Remarkable Reaction Rate and Excellent Enantioselective Direct α‐Amination of Aldehydes with Azodicarboxylates Catalyzed by Pyrrolidinylcamphor‐Derived Organocatalysts
2009
·
Pang‐Min Liu
, Chihliang Chang
, et al.
·
European Journal of Organic Chemistry
·
38
PDF
An efficient Morita–Baylis–Hillman reaction for the synthesis of multifunctional 2-hydroxy-3-nitrobut-3-enoate derivatives
2010
·
Hsuan-Hao Kuan
, Raju Jannapu Reddy
, et al.
·
Tetrahedron
·
32
Interrupted CuAAC‐Thiolation for the Construction of 1,2,3‐Triazole‐Fused Eight‐Membered Heterocycles from O ‐/ N ‐Propargyl derived Benzyl Thiosulfonates with Organic Azides
2021
·
Raju Jannapu Reddy
, Md. Waheed
, et al.
·
Advanced Synthesis & Catalysis
·
31
An Efficient Sequential One‐Pot Approach for the Synthesis of C3‐Functionalized Imidazo[1,2‐a]pyridines under Transition‐Metal Free Conditions
2019
·
Raju Jannapu Reddy
, Angothu Shankar
, et al.
·
Asian Journal of Organic Chemistry
·
31
An efficient synthesis of 4,5-disubstituted-2 H -1,2,3-triazoles from nitroallylic derivatives via a cycloaddition–denitration process
2017
·
Raju Jannapu Reddy
, Md. Waheed
, et al.
·
New Journal of Chemistry
·
30
General Entry into o‐,o′‐Heteroatom‐Linked N‐(Hetero)aryl‐Imidazole Motifs by Gold‐Catalysed Formal [3+2]‐Dipolar Cycloaddition
2017
·
Miguel Garzón
, Elsa M. Arce
, et al.
·
Advanced Synthesis & Catalysis
·
29
Synthesis of the 1-Phenethyltetrahydroisoquinoline Alkaloids (+)-Dysoxyline, (+)-Colchiethanamine, and (+)-Colchiethine
2012
·
Raju Jannapu Reddy
, Nobuyuki Kawai
, et al.
·
The Journal of Organic Chemistry
·
29
TiCl4 catalyzed tandem construction of C–C and C–O bonds: a simple and one-pot atom-economical stereoselective synthesis of spiro-oxindoles
2005
·
Deevi Basavaiah
, Jamjanam Srivardhana Rao
, et al.
·
Chemical Communications
·
28
Base-mediated [3 + 2]-cycloannulation strategy for the synthesis of pyrazolo[1,5- a ]pyridine derivatives using ( E )-β-iodovinyl sulfones
2022
·
Raju Jannapu Reddy
, Nunavath Sharadha
, et al.
·
Organic & Biomolecular Chemistry
·
27
Simple and facile synthesis of tetralone-spiro-glutarimides and spiro-bisglutarimides from Baylis–Hillman acetates
2008
·
Deevi Basavaiah
, Raju Jannapu Reddy
·
Organic & Biomolecular Chemistry
·
27
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Works count:
107
Citation count:
2,117
H-index:
26
I10-index:
39
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