Katsumasa Nonoshita

Amphiphilic reactions by means of exceptionally bulky organoaluminum reagents. Rational approach for obtaining unusual equatorial, anti-Cram, and 1,4 selectivity in carbonyl alkylation

Keiji Maruoka, Takayuki Itoh, Minoru Sakurai et al. · Journal of the American Chemical Society · 1988 · 218 citations

Amphiphilic Reactions, Molecular Sciences, Engineering +14

Organoaluminum-promoted Claisen rearrangement of allyl vinyl ethers

Katsumasa Nonoshita, Hiroshi Banno, Keiji Maruoka et al. · Journal of the American Chemical Society · 1990 · 143 citations

Altmetrics, Engineering, Donut Icon +12

Unprecedented stereochemical control in the Claisen rearrangement of allyl vinyl ethers using organoaluminum reagents

Keiji Maruoka, Katsumasa Nonoshita, Hiroshi Banno et al. · Journal of the American Chemical Society · 1988 · 61 citations

Unprecedented Stereochemical Control, Asymmetric Catalysis, Alkene Metathesis +11

Unusual conjugate addition of organolithium reagent to α, β-unsaturated ketone

Keiji Maruoka, Katsumasa Nonoshita, Hisashi Yamamoto · Tetrahedron Letters · 1987 · 58 citations

Engineering, Biochemistry, Natural Sciences +6

(9<i>S</i>)-9-(2-Hydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)-3,3-dimethyl-2,3,4,9-tetrahydro-1<i>H</i>-xanthen-1-one, a Selective and Orally Active Neuropeptide Y Y5 Receptor Antagonist

Nagaaki Sato, Makoto Jitsuoka, Takunobu Shibata et al. · Journal of Medicinal Chemistry · 2008 · 56 citations · Full text