Substitution reactions which proceed via radical anion intermediates. Part 27. A new reaction of .alpha.-nitro nitriles: conversion to .beta.-nitro nitriles
Copper-Catalyzed Alkylation of Nitroalkanes with α-Bromonitriles: Synthesis of β-Cyanonitroalkanes
作者:Kirk W. Shimkin、Peter G. Gildner、Donald A. Watson
DOI:10.1021/acs.orglett.6b00093
日期:2016.3.4
Copper catalysis now enables the efficient C-alkylation of nitroalkanes with α-bromonitriles. Using a simple and inexpensive catalyst, this process provides access to β-cyanonitroalkanes. The method is highly tolerant of various functional groups and substitution patterns. These functionally dense products serve as orthogonally masked 1,3-diamines, which can be revealed selectively for access to differentially
KORNBLUM, N.;SINGH, H. K.;BOYD, S. D., J. ORG. CHEM., 1984, 49, N 2, 358-362
作者:KORNBLUM, N.、SINGH, H. K.、BOYD, S. D.
DOI:——
日期:——
Substitution reactions which proceed via radical anion intermediates. Part 27. A new reaction of .alpha.-nitro nitriles: conversion to .beta.-nitro nitriles
作者:Nathan Kornblum、Haribansh K. Singh、Steven D. Boyd