Kentoku Gotanda

Facile and Efficient Sulfenylation Method Using Quinone Mono-<i>O,S</i>-Acetals under Mild Conditions

Masato Matsugi, Kenji Murata, Kentoku Gotanda et al. · The Journal of Organic Chemistry · 2001 · 122 citations

Chemical Engineering, Medicinal Chemistry, Novel Sulfenylation Method +13

Additions of malononitrile radicals to alkenes under mild conditions using 2,2′-azobis-(2,4-dimethyl-4-methoxyvaleronitrile) (V-70) as an initiator

Yasuyuki Kita, Atsunori Sano, Takahiro Yamaguchi et al. · Tetrahedron Letters · 1997 · 69 citations

Alkene Metathesis, Mild Conditions, Organic Chemistry +4

Design, Synthesis, and 1,3-Dipolar Cycloaddition of (5<i>R</i>)- [and (5<i>S</i>)]-5,6-Dihydro-5-phenyl-2<i>H</i>-1,4-oxazin-2-one <i>N</i>-Oxides as Chiral (<i>E</i>)-Geometry-Fixed α-Alkoxycarbonylnitrones

Osamu Tamura, Kentoku Gotanda, Jun Yoshino et al. · The Journal of Organic Chemistry · 2000 · 59 citations

Chemical Engineering, Engineering, Heterocyclic +11

Isolation of the Quinone Mono <i>O,S</i>‐Acetal Intermediates of the Aromatic Pummerer‐Type Rearrangement of <i>p</i>‐Sulfinylphenols with 1‐Ethoxyvinyl Esters

Yasuyuki Kita, Yoshifumi Tekeda, Masato Matsugi et al. · Angewandte Chemie International Edition in English · 1997 · 51 citations

Asymmetric Catalysis, Engineering, Aromatic Pummerer‐type Rearrangement +12

Practical Radical Additions under Mild Conditions Using 2,2‘-Azobis(2,4-dimethyl-4-methoxyvaleronitrile) [V-70] as an Initiator

Yasuyuki Kita, Kentoku Gotanda, Kenji Murata et al. · Organic Process Research & Development · 1998 · 50 citations