Biotransformation of organic sulfides. Part 7. Formation of chiral isothiocyanato sulfoxides and related compounds by microbial biotransformation

Design and synthesis of bifunctional isothiocyanate analogs of sulforaphane: correlation between structure and potency as inducers of anticarcinogenic detoxication enzymes

Gary H. Posner, C.-G. Cho, Julianne V. Green et al. · Journal of Medicinal Chemistry · 1994 · 158 citations

Stereochemical analysis of sulfoxides obtained by diverted desaturation

Peter H. Buist, Dale M. Marecak · Journal of the American Chemical Society · 1992 · 88 citations

Bioorganic Chemistry, Engineering, Chemical Analysis +16

Asymmetric Synthesis of Chiral Sulfinate Esters and Sulfoxides. Synthesis of Sulforaphane

James K. Whitesell, Man Shing Wong · The Journal of Organic Chemistry · 1994 · 60 citations

Chiral Sulfinate Esters, Chemical Engineering, Engineering +11

(S)-α-methoxyphenyl acetic acid : a new NMR chiral shift reagent for the stereochemical analysis of sulfoxides

Peter H. Buist, Dale M. Marecak, Herbert L. Holland et al. · Tetrahedron Asymmetry · 1995 · 44 citations

Biochemistry, Natural Sciences, Organic Chemistry +6

Microbial oxidation of benzyl sulfides and bibenzyl by <i>Mortierella</i> <i>isabellina</i> and <i>Helminthosporium</i> species

Herbert L. Holland, Cynthia G. Rand, Péter Viski et al. · Canadian Journal of Chemistry · 1991 · 43 citations · Full text

Microbial Physiology, Organic Chemistry, Chemistry +17