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Jack E. Baldwin

Dyson Perrins Laboratory

Oxford University

South Parks Road

Oxford OX1 3QY

UK

[email]@chem.ox.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Dyson Perrins Laboratory, Oxford University, South Parks Road, Oxford OX1 3QY, UK. 2002
  • The Dyson Perrins Laboratory, University of Oxford, U.K. 1999 - 2001

References

  1. Total synthesis of pyridovericin: studies toward the biomimetic synthesis of pyridomacrolidin. Baldwin, J.E., Adlington, R.M., Conte, A., Irlapati, N.R., Marquez, R., Pritchard, G.J. Org. Lett. (2002) [Pubmed]
  2. Parallel synthesis of novel heteroaromatic acromelic acid analogues from kainic acid. Baldwin, J.E., Fryer, A.M., Pritchard, G.J. J. Org. Chem. (2001) [Pubmed]
  3. 1H NMR study of protected and unprotected kainoid amino acids: facile assignment of C-4 stereochemistry. Baldwin, J.E., Fryer, A.M., Pritchard, G.J. J. Org. Chem. (2001) [Pubmed]
  4. Studies toward the total synthesis of the cytotoxic sponge alkaloid pyrinodemin A. Baldwin, J.E., Romeril, S.P., Lee, V., Claridge, T.D. Org. Lett. (2001) [Pubmed]
  5. Novel C-4 heteroaromatic kainoid analogues: a parallel synthesis approach. Baldwin, J.E., Fryer, A.M., Pritchard, G.J. Bioorg. Med. Chem. Lett. (2000) [Pubmed]
  6. The synthesis of 4-arylsulfanyl-substituted kainoid analogues from trans-4-hydroxy-L-proline. Baldwin, J.E., Pritchard, G.J., Williamson, D.S. Bioorg. Med. Chem. Lett. (2000) [Pubmed]
  7. Studies toward the biomimetic synthesis of tropolone natural products via a hetero Diels-Alder reaction. Baldwin, J.E., Mayweg, A.V., Neumann, K., Pritchard, G.J. Org. Lett. (1999) [Pubmed]
 
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