Nagaraj R. Ayyangar

Hydroboration. XVIII. The Reaction of Diisopinocampheylborane with Representative <i>cis</i>-Acyclic, Cyclic, and Bicyclic Olefins. A Convenient Systhesis of Optically Active Alcohols and Olefins of High Optical Purity and Established Configuration

Herbert C. Brown, Nagaraj R. Ayyangar, George Zweifel · Journal of the American Chemical Society · 1964 · 125 citations

Derivative (Chemistry), Engineering, Altmetric Attention Score +11

Hydroboration. XIX. The Reaction of Dissopinocampheylborane with Representative <i>trans</i> andHindered Olefins. Triisopinocampheyldiborane as a Reagent for the Configurational Assignment of Alcohols and Olefins <i>via</i> Hydroboration

Herbert C. Brown, Nagaraj R. Ayyangar, George Zweifel · Journal of the American Chemical Society · 1964 · 51 citations

Derivative (Chemistry), Engineering, Chemical Analysis +9

<b>Hydroboration. XVII. An Examination of Several Representative Dialkylboranes as Selective Hydroborating Agents</b>

George Zweifel, Nagaraj R. Ayyangar, Herbert C. Brown · Journal of the American Chemical Society · 1963 · 41 citations

Chemical Engineering, Chemical Measurement, Engineering +9

New reactions of polyfluoroaromatic compounds. Pentafluorophenylalanine and tetrafluorotyrosine

Robert Filler, Nagaraj R. Ayyangar, Wlodzimierz Gustowski et al. · The Journal of Organic Chemistry · 1969 · 39 citations

Donut Icon, Altmetric Attention Score, Fluorous Synthesis +7

An efficient entry into butenolides: Synthesis of (±) mintlactone

Subhash P. Chavan, P. K. Zubaidha, Nagaraj R. Ayyangar · Tetrahedron Letters · 1992 · 36 citations

Efficient Entry, Enantioselective Synthesis, Chemistry +1