Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Robin P. Attrill"'
Autor:
John K. Roberts, and Martin J. Teasdale, Robin P. Attrill, John Edward Richardson, Andre Wanders, Keith R. Mulholland, Mark A. Blower
Publikováno v:
Organic Process Research & Development. 4:98-101
The development of a pilot plant process to prepare the spirocyclic piperidine (2) from the tetrahydropyridine (4) via a radical cyclisation reaction is described. The pilot plant process involves the use of a catalytic amount of tributyltin hydride
Publikováno v:
Synthetic Communications. 29:827-833
The one-pot condensation of N-methylhomoveratrylamine with acrolein followed by in situ reductive amination with 3,4-dimethoxyaniline to give an unsymmetrical propane 1,3-diamine in excellent yield is described.
Publikováno v:
ChemInform. 30
The one-pot condensation of N-methylhomoveratrylamine with acrolein followed by in situ reductive amination with 3,4-dimethoxyaniline to give an unsymmetrical propane 1,3-diamine in excellent yield is described.
Autor:
Walter J. Smith, Edward K. Chess, Michael L. Vieira, Michal Sabat, Robin P. Attrill, John H. C. Nayler, Kirk A. Ashline, Jeremy R. Everett, David E. Pereira, J. Peter Clayton, Ernest A. Cutmore, John W. Tyler
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1559
High-field nuclear magnetic resonance spectroscopy, mass spectrometry, infrared spectroscopy, and ultraviolet spectroscopy were used to determine the structures of two novel degradation productions of the penicillins sodium nafcillin (1) and sodium o
Autor:
Michael J. Betts, John D. Buynak, Ramalakshmi Yegna Chandrasekaran, Robin P. Attrill, Anthony G. M. Barrett
Publikováno v:
The Journal of Organic Chemistry. 50:5362-5365
Autor:
Michael J. Betts, Robin P. Attrill, Peter Quayle, Jan Van der Westhuizen, Anthony G. M. Barrett
Publikováno v:
The Journal of Organic Chemistry. 49:1679-1682
L'acetoxy-4 trimethylsilyl-1 azetidinone-2 reagit avec divers enols ethers de silicium dans le dichloromethane en presence de triflate de trimethylsilyle pour donner des phenacyl-4 azetidinones-2, et α-methyl- ou α-acetyl oxo-4 azetidineacetates-2,