Stereospecific Michael addition of dithioester enethiolates with acyclic enones

The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation

Robert E. Ireland, Richard H. Mueller, Alvin K. Willard · Journal of the American Chemical Society · 1976 · 807 citations

Engineering, Biochemistry, Natural Sciences +12

Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis

Paul A. Bartlett · Tetrahedron · 1980 · 506 citations

Acyclic Systems, Natural Sciences, Diversity-oriented Synthesis +7

Synthesis of Open‐Chain 2,3‐Disubstituted 4‐nitroketones by Diastereoselective <i>Michael</i>‐addition of (<i>E</i>)‐Enamines to (<i>E</i>)‐Nitroolefins. A topological rule for C, C‐bond forming processes between prochiral centres. Preliminary communication

Dieter Seebàch, J. GOLINSKI · Helvetica Chimica Acta · 1981 · 375 citations

Engineering, Diene Synthesis, Natural Sciences +14

Stereo- and regiochemistry of the Claisen rearrangement: applications to natural products synthesis

Frederick E. Ziegler · Accounts of Chemical Research · 1977 · 254 citations

Altmetrics, Natural Products Synthesis, Engineering +15

Acyclic stereoselection. 29. Stereoselection in the Michael addition reaction. 1. The Mukaiyama-Michael reaction

Clayton H. Heathcock, Mark H. Norman, David Uehling · Journal of the American Chemical Society · 1985 · 99 citations

Altmetrics, Engineering, Donut Icon +11