Results 1 - 10 of 73 (Click here to explore results)

1

Efficient synthesis of chiral benzofuryl β-amino alcohols via a catalytic asymmetric Henry reaction. Wei Chen, Zhao-Hui Zhou, Hong-Bin Chen , Org. Biomol. Chem. , 2017 , 15 , 1530

Bromopicrin reaction. Part II. Reaction between 2-nitroethanol and sodium hypobromite. Ross I. Aylott, Anthony R. Butler, David S. B. Grace, Hamish McNab , J. Chem. Soc., Perkin Trans. 2 , 1973 , 1107

Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids. Ponmuthu Kottala Vijaya, Sepperumal Murugesan, Ayyanar Siva , Org. Biomol. Chem. , 2016 , 14 , 10101

The reaction of geminal bromonitroalkanes with nucleophiles. Part 1. The decomposition of 2-bromo-2-nitropropane-1,3-diol (‘Bronopol’) in aqueous base. Brian C. Challis, Taher I. Yousaf , J. Chem. Soc., Perkin Trans. 2 , 1991 , 283

A new route to racemic erythro-sphingosine and ceramides. The 1,2-versus 1,4-addition reaction of hexadec-2-enal with 2-nitroethanol. Tohru Hino, Kiyoshi Nakakyama, Mikio Taniguchi, Masako Nakagawa , J. Chem. Soc., Perkin Trans. 1 , 1986 , 1687

241. Addition of dinitrogen tetroxide to olefins. Part II. Ethylene. Norman Levy, Charles W. Scaife, Arthur E. Wilder Smith , J. Chem. Soc. , 1946 , 1096

An ionic liquid gel: a heterogeneous catalyst for Erlenmeyer–Plochl and Henry reactions. Megha Jagadale, Altafhusen Naikwade, Rajashri Salunkhe, Mohan Rajmane, Gajanan Rashinkar , New J. Chem. , 2018 , 42 , 10993

Nucleophilic substitution at bivalent sulphur. Part V. A study of exchange reactions at bivalent sulphur using ¹⁹F nuclear magnetic resonance spectroscopy. Donald R. Hogg, Joseph Stewart , J. Chem. Soc., Perkin Trans. 2 , 1974 , 1040

The mass spectrometry of nitrate esters and related compounds. Part II. R. T. M. Fraser, N. C. Paul , J. Chem. Soc. B , 1968 , 1407

Synthesis and antiproliferative effect of the proposed stereoisomer of the marine sponge metabolite halisphingosine A. Alexander Bär, Sofia I. Bär, Rainer Schobert , Org. Biomol. Chem. , 2020 , 18 , 7565