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- Publications
- Influence
A second-generation catalyst for intermolecular hydroacylation of alkenes and alkynes using beta-S-substituted aldehydes: the role of a hemilabile P-O-P ligand.
- Gemma L. Moxham, Helen E. Randell-Sly, S. Brayshaw, R. L. Woodward, A. Weller, M. Willis
- Chemistry, Medicine
- Angewandte Chemie
- 20 November 2006
Rhodium-catalyzed intermolecular chelation controlled alkene and alkyne hydroacylation: synthetic scope of beta-S-substituted aldehyde substrates.
- M. Willis, Helen E. Randell-Sly, R. L. Woodward, S. McNally, G. Currie
- Chemistry, Medicine
- The Journal of organic chemistry
- 9 June 2006
The use of beta-S-substituted aldehydes in rhodium-catalyzed intermolecular hydroacylation reactions is reported. Aldehydes substituted with either sulfide or thioacetal groups undergo efficient… Expand
Catalytic enantioselective total synthesis of hodgkinsine B.
- R. Snell, R. L. Woodward, M. Willis
- Chemistry, Medicine
- Angewandte Chemie
- 19 September 2011
Chelation-controlled intermolecular alkene and alkyne hydroacylation: the utility of beta-thioacetal aldehydes.
- M. Willis, Helen E. Randell-Sly, R. L. Woodward, G. Currie
- Chemistry, Medicine
- Organic letters
- 3 May 2005
[reaction: see text]. Beta-thioacetal-substituted aldehydes, which are conveniently prepared from the corresponding ynals, can be combined with a range of alkynes or electron-poor alkenes to deliver… Expand
End-result Measurements of the Quality of Obstetrical Care in Two U. S. Air Force Hospitals
- J. Thompson, D. Marquis, R. L. Woodward, Richard C. Yeomans
- Medicine
- 1 March 1968
THIS IS A REPORT of a comparative study of the quality of obstetrical care in two different medical institutions, in this case hospitals. Because the hospitals are operated by one of the Armed… Expand
Catalytic enantioselective desymmetrisation as a tool for the synthesis of hodgkinsine and hodgkinsine B.
- R. Snell, M. J. Durbin, R. L. Woodward, M. Willis
- Chemistry, Medicine
- Chemistry
- 21 December 2012
Two palladium-catalysed amination protocols are deployed in the desymmetrisation of the complex dimeric alkaloid meso-chimonanthine. The power of these transformations is showcased in an efficient… Expand
Rhodium-catalyzed reductive aldol reactions using aldehydes as the stoichiometric reductants.
- M. Willis, R. L. Woodward
- Chemistry, Medicine
- Journal of the American Chemical Society
- 3 December 2005
Chelated acyl rhodium hydrides, generated from the addition of [Rh(dppe)]ClO4 to beta-sulfide-substituted aldehydes, can function as the stoichiometric reductants in reductive aldol processes.… Expand
Scalar coupling between the 15N centres in methylated 1,8-diaminonaphthalenes and 1,6-diazacyclodecane: to what extent is 2HJNN a reliable indicator of N-N distance?
- G. Lloyd-Jones, J. Harvey, Paul Hodgson, M. Murray, R. L. Woodward
- Chemistry, Medicine
- Chemistry
- 22 September 2003
The scalar couplings between hydrogen bonded nitrogen centres ((2H)J(NN)) in the free-base and protonated forms of the complete series of [(15)N(2)]-N-methylated 1,8-diamino naphthalenes in [D(7)]DMF… Expand
Entropy-driven hydrogen bonding: stereodynamics of a protonated, N,N-chiral "proton sponge".
- P. Hodgson, G. Lloyd-Jones, M. Murray, T. Peakman, R. L. Woodward
- Chemistry, Medicine
- Chemistry
- 15 December 2000
The C2-symmetric ("[DL]") and achiral ("[meso]") diastereoisomers of the hydrogen iodide salt of 1,8-bis-(N-benzyl-N-methylamino)naphthalene ([2H]-[I] ) interconvert in solution. Direct… Expand
Tandem palladium-catalyzed urea arylation-intramolecular ester amidation: regioselective synthesis of 3-alkylated 2,4-quinazolinediones.
- M. Willis, R. Snell, A. J. Fletcher, R. L. Woodward
- Chemistry, Medicine
- Organic letters
- 26 September 2006
o-Halo benzoates can be combined with monoalkyl ureas in a tandem palladium-catalyzed arylation-ester amidation sequence to deliver quinazolinedione products. The reactions are regioselective for… Expand