D. Reddeppa Reddy

A very mild, catalytic and versatile procedure for α-oxidation of ketone silyl enol ethers using (salen)manganese(<scp>III</scp>) complexes; a new, chiral complex giving asymmetric induction. A possible model for selective biochemical oxidative reactions through enol formation

D. Reddeppa Reddy, Edward R. Thornton · Journal of the Chemical Society Chemical Communications · 1992 · 71 citations

Natural Sciences, Chemical Engineering, Chemistry +14

Methodology for the synthesis of the spiro[4.4]nonane system: an approach for the total synthesis of fredericamycin A

A. V. R. RAO, D. Reddeppa Reddy, V. H. DESHPANDE · Journal of the Chemical Society Chemical Communications · 1984 · 15 citations

Natural Sciences, Chemistry, Medicinal Chemistry +9

Regiospecific synthesis of 9-ethoxy-4,5,6,8-tetramethoxy-1,3-dihydro-naphtho-(2,3-) furan-1-one: A key synthon of fredericamycin A

AV Rama Rao, N. SREENIVASAN, D. Reddeppa Reddy et al. · Tetrahedron Letters · 1987 · 15 citations

Natural Sciences, Chemistry, Medicinal Chemistry +9

Synthesis of 4,9-diethoxy-5,6,(7),8-trimethoxy-1,3-dihydronaphtho-(2,3-)-furan-1-one: A key synthon of fredericamycin A

AV Rama Rao, D. Reddeppa Reddy, G. S. Annapurna et al. · Tetrahedron Letters · 1987 · 14 citations

Natural Sciences, Chemistry, Medicinal Chemistry +8