Substituent effects in the reaction of allyl trichloroacetimidates with N-halosuccinimides: Cyclization vs aza-Claisen rearrangement

Methods of Organic Chemistry

J. W. Cook · Nature · 1954 · 321 citations · Full text

Natural Sciences, Chemistry, Analytical Chemistry +8

Mercury(<scp>II</scp>)‐ and Palladium(<scp>II</scp>)‐Catalyzed [3,3]‐Sigmatropic Rearrangements [New Synthetic Methods (46)]

Larry E. Overman · Angewandte Chemie International Edition in English · 1984 · 317 citations

Natural Sciences, Chemistry, Catalysis +9

A general method for the synthesis of amines by the rearrangement of allylic trichloroacetimidates. 1,3 Transposition of alcohol and amine functions

Larry E. Overman · Journal of the American Chemical Society · 1976 · 291 citations

Natural Sciences, Chemistry, Organic Chemistry +5

Allylic and propargylic imidic esters in organic synthesis

Larry E. Overman · Accounts of Chemical Research · 1980 · 249 citations

Natural Sciences, Chemistry, Bioisosterism +5

Preparation of peptidic α-hydroxy phosphonates a new class of transition state analog renin inhibitors

Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono · Tetrahedron Letters · 1990 · 237 citations

Pharmacy, Medicinal Chemistry, Pharmacology +12