Ronald S. Lenox

Generation of allyllithium reagents by lithium-tetrahydrofuran reduction of allylic mesitoates. New procedure for selective allylic cross coupling and allylcarbinol synthesis

John A. Katzenellenbogen, Ronald S. Lenox · The Journal of Organic Chemistry · 1973 · 76 citations

Natural Sciences, Chemistry, Green Chemistry +7

Stereoselective method for the synthesis of both olefinic isomers from a single precursor. Conjugate reduction of .alpha.,.beta.-unsaturated epoxides

Ronald S. Lenox, John A. Katzenellenbogen · Journal of the American Chemical Society · 1973 · 53 citations

Natural Sciences, Chemistry, Analytical Chemistry +8

Improved synthesis of 2-methyl-6-methylene-2,7-octadien-4-ol, a pheromone of Ips paraconfusus, and an alternative synthesis of the intermediate, 2-bromomethyl-1,3-butadiene

Robert G. Riley, Robert M. Silverstein, John A. Katzenellenbogen et al. · The Journal of Organic Chemistry · 1974 · 45 citations

Natural Sciences, Chemistry, Bioisosterism +6

Educating for the serendipitous discovery

Ronald S. Lenox · Journal of Chemical Education · 1985 · 27 citations

Management, Educational Measurement, Information Retrieval +5

Synthesis of 4-lithio-2-methyl-2-pentene. A new type of allylic organometallic compound

Thomas E. Stanberry, Michael J. Darmon, Herbert A. Fry et al. · The Journal of Organic Chemistry · 1976 · 14 citations

Natural Sciences, Chemistry, Natural Product Biosynthesis +6