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Nitrile biosynthesis in nature: how and why? . Mingyu Liu, Shengying Li
, Nat. Prod. Rep.
, 2024
, 41
, 649
Biocatalytic asymmetric ring-opening of dihydroisoxazoles: a cyanide-free route to complementary enantiomers of β-hydroxy nitriles from olefins . Daijun Zheng, Yasuhisa Asano
, Green Chem.
, 2020
, 22
, 4930
Chemistry, biosynthesis and biology of floral volatiles: roles in pollination and other functions . Stefan Dötterl, Jonathan Gershenzon
, Nat. Prod. Rep.
, 2023
, 40
, 1901
Chemoenzymatic one-pot reaction from carboxylic acid to nitrile via oxime . Melissa Horvat, Victoria Weilch, Robert Rädisch, Sebastian Hecko, Astrid Schiefer, Florian Rudroff, Birgit Wilding, Norbert Klempier, Miroslav Pátek, Ludmila Martínková, Margit Winkler
, Catal. Sci. Technol.
, 2022
, 12
, 62
Stabilisation of copper(I ) by an azoimine ligand: redox properties and reactions of bis(phenylazoacetaldoximato)bis(phenylacetaldoxime)dicopper(I ) . Samudranil Pal, Debkumar Bandyopadhyay, Dipankar Datta, Animesh Chakravorty
, J. Chem. Soc., Dalton Trans.
, 1985
, 159
Some dimeric by-products of the preparation of 2,4-dimethoxybenzyl cyanide from 2,4-dimethoxy-β-nitrostyrene . W. D. P. Burns, W. Cocker, T. B. H. McMurry, P. A. Staniland
, J. Chem. Soc. C
, 1967
, 1554
Indium mediated allylation of glyoxylate oxime ethers , esters and cyanoformates . Dougal J. Ritson, Russell J. Cox, John Berge
, Org. Biomol. Chem.
, 2004
, 2
, 1921
Chiral oxime ethers in asymmetric synthesis. Part 4. Asymmetric synthesis of N -protected amines and β-amino acids by the addition of organometallic reagents to ROPHy/SOPHy-derived aldoximes . James C. A. Hunt, Cephas Lloyd, Christopher J. Moody, Alexandra M. Z. Slawin, Andrew K. Takle
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 3443
Synthesis of imidazole 1-oxides from 1,2-diimines . Jesús Alcázar, Mikael Begtrup, Antonio de la Hoz
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 2467
Water-mediated decarboxylative radical nitrosation of β-keto acids with tert -butyl nitrite: access to α-oximino ketones . Lina Jia, Linlin Li, Fuzhong Han, Xiangping Hu
, New J. Chem.
, 2022
, 46
, 22045