Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mandy Parsons"'
Autor:
Kyle B. Bills, J.Daniel Obray, Travis Clarke, Mandy Parsons, James Brundage, Chae Ha Yang, Hee Young Kim, Jordan T. Yorgason, Jonathan D. Blotter, Scott C. Steffensen
Publikováno v:
Brain Stimulation, Vol 13, Iss 2, Pp 403-411 (2020)
Background: Growing evidence suggests that mechanical stimulation modulates substrates in the supraspinal central nervous system (CNS) outside the canonical somatosensory circuits.Objective/Methods: We evaluate mechanical stimulation applied to the c
Externí odkaz:
https://doaj.org/article/e7a64d90d2e84451b2a3663d0ddb6d04
Autor:
Richard D. Chambers, Graham Sandford, Mandy Parsons, Judith A. K. Howard, Takashi Nakano, Andrei S. Batsanov
Publikováno v:
Journal of Fluorine Chemistry. 129:811-816
Reactions of 3β-acetoxy-5α-androstan-17-one with elemental fluorine and Selectfluor® are reported and give contrasting results. Fluorine gives a mixture of mono-fluorinated steroids in which fluorine atoms are attached to tertiary carbon sites whe
Autor:
Emmanuelle Thomas, Jelena Trmcic, John S. Moilliet, Graham Sandford, Richard D. Chambers, Mandy Parsons
Publikováno v:
Tetrahedron. 62:7162-7167
Reaction of a series of model hexyl derivatives of the form C6H13–X (X=Cl, Br, I, CO2Me, COMe, CHO) with both elemental fluorine and Selectfluor™ was studied in order to assess the impact of electron withdrawing functional groups upon fluorinatio
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2190-2197
Selective fluorination of a range of hydrocarbons was achieved by reaction with either elemental fluorine or Selectfluor™, an electrophilic fluorinating reagent of the N–F class. An electrophilic mechanism is envisaged. On prolonged reaction, the
Autor:
Richard D. Chambers, Mandy Parsons, John S. Moilliet, Christopher John Skinner, Malcolm J. Atherton, Graham Sandford
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :803-810
Selective fluorination of a range of pyridine and quinoline substrates to give corresponding 2-fluoro-derivatives can be readily achieved in high yield at room temperature using elemental fluorine–iodine mixtures. Reaction of fluorine with iodine f
Publikováno v:
ChemInform. 34
Publikováno v:
ChemInform. 31
Transformation of carbon–hydrogen bonds to carbon–fluorine bonds at saturated secondary and tertiary carbon sites by electrophilic aliphatic substitution processes is possible using either elemental fluorine or fluorinating reagents of the N–F
Publikováno v:
Chemical Communications. :959-960
Transformation of carbon–hydrogen bonds to carbon–fluorine bonds at saturated secondary and tertiary carbon sites by electrophilic aliphatic substitution processes is possible using either elemental fluorine or fluorinating reagents of the N–F
Autor:
Yoowannakul, Suree, Vongsanim, Surachet, Tangvoraphonkchai, Kamonwan, Mohamed, Ahmed, Davenport, Andrew
Publikováno v:
Renal Replacement Therapy; 1/7/2020, Vol. 6 Issue 1, p1-8, 8p
Autor:
D. Chambers, Richard, Parsons, Mandy, Sandford, Graham, J. Skinner, Christopher, J. Atherton, Malcolm, S. Moilliet, John
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1 (0300922X); 1999, Issue 7, p803-810, 1p