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- Active site modifications in pentaerythritol tetranitrate reductase can lead to improved product enantiopurity, decreased by-product formation and altered stereochemical outcome in reactions with α,β-unsaturated nitroolefins. Anna Fryszkowska, Helen Toogood, Michiyo Sakuma, Gill M. Stephens, John M. Gardiner, Nigel S. Scrutton
, Catal. Sci. Technol.
, 2011
, 1
, 948
- Ψ[CH(CF3)NH]Gly-peptides: synthesis and conformation analysis. Marco Molteni, Maria Cristina Bellucci, Serena Bigotti, Stefania Mazzini, Alessandro Volonterio, Matteo Zanda
, Org. Biomol. Chem.
, 2009
, 7
, 2286
- Bicycloannulation with nitroethene and 1-nitropropene. A one-step synthesis of tricyclenone. Robert M. Cory, Paul C. Anderson, Fred R. McLaren, Brian R. Yamamoto
, J. Chem. Soc., Chem. Commun.
, 1981
, 73
- Recent advancement in the synthesis of diverse spiro-indeno[1,2-b]quinoxalines: a review. Ruby Singh, Diksha Bhardwaj, Munna Ram Saini
, RSC Adv.
, 2021
, 11
, 4760
- Synthesis of 3-vinylisoxazole by a nitrile oxide cycloaddition/Diels–Alder cycloreversion pathway. Philip W. Ambler, R. Michael Paton, Jaki M. Tout
, J. Chem. Soc., Chem. Commun.
, 1994
, 2661
- He I and He II photoelectron spectra of isomeric nitropropenes. W. S. Chin, C. Y. Mok, H. H. Huang
, J. Chem. Soc., Faraday Trans.
, 1991
, 87
, 1685
- Metal organic frameworks mimicking natural enzymes: a structural and functional analogy. Ipsita Nath, Jeet Chakraborty, Francis Verpoort
, Chem. Soc. Rev.
, 2016
, 45
, 4127
- Synthesis and practical applications of 2-(2-nitroalkyl)pyrroles. Alessandro Palmieri, Marino Petrini
, Org. Biomol. Chem.
, 2020
, 18
, 4533
- Zeolite Y-assisted nitration of aromatic and heterocyclic compounds and decarboxylative nitration of α,β-unsaturated acids under non-conventional conditions. V. Sudhakar Chary, K. C. Rajanna, G. Krishnaiah, P. Srinivas
, Catal. Sci. Technol.
, 2016
, 6
, 1430
- Direct reductive coupling of indoles to nitrostyrenes en route to (indol-3-yl)acetamides. Alexander V. Aksenov, Nicolai A. Aksenov, Zarema V. Dzhandigova, Dmitrii A. Aksenov, Leonid G. Voskressensky, Valentine G. Nenajdenko, Michael Rubin
, RSC Adv.
, 2016
, 6
, 93881