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Dr D Basavaiah

vidwan id: 113157
Male

Professor, School of Chemistry
University of Hyderabad

Expertise

  • Multidisciplinary Chemistry

Publications

Total Articles 147
Books 0
Proceedings 0

Publications

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Scopus

Citations 9228
h-index 43

CrossRef

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Citations 6985
h-index 35
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Bio

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Personal Details

  • Male
  • Professor , University of Hyderabad
  • University of Hyderabad
Ph.D
Banaras Hindu University 1979
M.Sc
Banaras Hindu University 1972
B.Sc
Andhra Loyola college, Vijayawada 1970
Professor Jul 1996 – Present
University of Hyderabad | School of Chemistry

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University of Rajasthan

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Dr Bakthadoss Manickam

Pondicherry University

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Pondicherry University

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Scholarly Work

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Scholarly Publications

Simple and facile synthesis of tetralone-spiro-glutarimides and spiro-bisglutarimides from Baylis-Hillman acetates

Open Access
Article

(5S)-1-Aza-2-imino-3-oxa-4,4-diphenylbicyclo(3.3.0)octane: a novel chiral catalytic source containing the N-(C{double bond, long}NH)-O moiety for the borane-mediated asymmetric reduction of prochiral ketones

Open Access
Article
Authors: Basavaiah D.;Venkateswara Rao K.;Sekhara Reddy B.

The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety

Open Access
Article

The Baylis-Hillman reaction: A novel source of attraction, opportunities, and challenges in synthetic chemistry

Open Access
Review
Authors: Basavaiah, Deevi;Venkateswara Rao, Kalapala;Jannapu Reddy, Raju
375

The Baylis–Hillman reaction: A novel source of attraction, opportunities, and challenges in synthetic chemistry

Open Access
Article

Chiral diamides as efficient catalytic precursors for the borane-mediated asymmetric reduction of prochiral ketones

Open Access
Article
Authors: Basavaiah D.;Venkateswara Rao K.;Sekhara Reddy B.

An expedient, facile and simple one-pot synthesis of 2-methylenealkanoates and alkanenitriles from the Baylis-Hillman bromides in aqueous media.

Open Access
Article

Simple and one-pot protocol for synthesis of indene-spiro-oxindoles involving tandem Prins and Friedel-Crafts reactions

Open Access
Article