Remarkable examples of double diastereodifferentiation: Application to the Eudistomin and Eudistomidin alkaloids

Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

Satoru Masamune, William Choy, John S. Petersen et al. · Angewandte Chemie International Edition in English · 1985 · 1.1K citations

Natural Sciences, Chemistry, Carbohydrate Chemistry +14

Eudistomins A-Q, .beta.-carbolines from the antiviral Caribbean tunicate Eudistoma olivaceum

Kenneth L. Rinehart, Jun’ichi Kobayashi, Gary C. Harbour et al. · Journal of the American Chemical Society · 1987 · 239 citations

Natural Sciences, Chemistry, Astrochemistry +9

Eudistomins C, E, K, and L, potent antiviral compounds containing a novel oxathiazepine ring from the Caribbean tunicate Eudistoma olivaceum

Kenneth L. Rinehart, Jun’ichi Kobayashi, Gary C. Harbour et al. · Journal of the American Chemical Society · 1984 · 185 citations

Natural Sciences, Chemistry, Medicinal Chemistry +12

Silicon in synthesis: stabase adducts - a new primary amine protecting group: alkylation of ethyl glycinate

Stevan W. Djurić, John J. Venit, Philip Magnus · Tetrahedron Letters · 1981 · 133 citations

Natural Sciences, Chemistry, Medicinal Chemistry +5

Eudistomidins B, C, and D: novel antileukemic alkaloids from the Okinawan marine tunicate Eudistoma glaucus

Jun’ichi Kobayashi, Jie‐Fei Cheng, Tomihisa Ohta et al. · The Journal of Organic Chemistry · 1990 · 122 citations

Natural Sciences, Marine Biology, Medicinal Chemistry +11