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- A radical based addition–elimination route for the preparation of indoles. John A. Murphy, Karen A. Scott, Rhona S. Sinclair, Concepcion Gonzalez Martin, Alan R. Kennedy, Norman Lewis
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2395
- Hypophosphite mediated carbon–carbon bond formation: total synthesis of epialboatrin and structural revision of alboatrin. Stephen R. Graham, John A. Murphy, Alan R. Kennedy
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 3071
- Binary complexes of tertiary amines with phenylacetylene. Dispersion wins over electrostatics. Surajit Maity, G. Naresh Patwari, S. Karthikeyan, Kwang S. Kim
, Phys. Chem. Chem. Phys.
, 2010
, 12
, 6150
- A stepwise one-pot synthesis of aliphatic thiols and their derivatives from acrylamides and sulfur. András Gy. Németh, Renáta Szabó, Krisztina Németh, György M. Keserű, Péter Ábrányi-Balogh
, Org. Biomol. Chem.
, 2022
, 20
, 4361
- Iodonium complexes of the tertiary amines quinuclidine and 1-ethylpiperidine. Jas S. Ward, Antonio Frontera, Kari Rissanen
, Dalton Trans.
, 2021
, 50
, 8297
- New reaction mode of the Horner–Wadsworth–Emmons
reaction using Sn(OSO2CF3)2 and
N-ethylpiperidine. Shigeki Sano, Kenji Yokoyama, Mari Fukushima, Tetsuo Yagi, Yoshimitsu Nagao
, Chem. Commun.
, 1997
, 559
- Tertiary amine
solvents having switchable hydrophilicity. Philip G. Jessop, Lisa Kozycz, Zahra Ghoshouni Rahami, Dylan Schoenmakers, Alaina R. Boyd, Dominik Wechsler, Amy M. Holland
, Green Chem.
, 2011
, 13
, 619
- Hollow nanostructures from self-assembled supramolecular metallo-triblock copolymers. Adam O. Moughton, Kurt Stubenrauch, Rachel K. O'Reilly
, Soft Matter
, 2009
, 5
, 2361
- Kinetic hydrogen isotope effects in the reaction between 2,4,6-trinitrotoluene and 1-ethylpiperidine in acetonitrile. The effect of pressure. Naoki Sugimoto, Muneo Sasaki
, J. Chem. Soc., Faraday Trans. 1
, 1985
, 81
, 2959
- Alkyl coupling in tertiary amines as analog of Guerbet condensation reaction. Yage Zhou, Dan Wu, Willinton Yesid Hernández, Changru Ma, Huangyang Su, Vitaly Ordomsky
, RSC Adv.
, 2019
, 9
, 9845