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- Antitumour imidazotetrazines. Part 33. New syntheses of the antitumour drug temozolomide using ‘masked’ methyl isocyanates. Yongfeng Wang, Malcolm F. G. Stevens, William T. Thomson, Bruce P. Shutts
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 2783
- An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions. Cheng-Guo Liu, Zheng-Yang Gu, Hui-Wen Bai, Shun-Yi Wang, Shun-Jun Ji
, Org. Chem. Front.
, 2016
, 3
, 1299
- A computationally designed binding mode flip leads to a novel class of potent tri-vector cyclophilin inhibitors. Alessio De Simone, Charis Georgiou, Harris Ioannidis, Arun A. Gupta, Jordi Juárez-Jiménez, Dahlia Doughty-Shenton, Elizabeth A. Blackburn, Martin A. Wear, Jonathan P. Richards, Paul N. Barlow, Neil Carragher, Malcolm D. Walkinshaw, Alison N. Hulme, Julien Michel
, Chem. Sci.
, 2019
, 10
, 542
- Alternative syntheses of the antitumlur drug temozolomide avoiding the use of methyl isocyanate. Yongfeng Wang, Malcolm F. G. Stevens, W. Thomson
, J. Chem. Soc., Chem. Commun.
, 1994
, 1687
- Amino-acids and peptides. Part XXXI. N-(piperidino-oxycarbonyl)-amino-acids and their use in peptide synthesis. D. Stevenson, G. T. Young
, J. Chem. Soc. C
, 1969
, 2389
- Antitumour imidazotetrazines. Part 39.1 Synthesis of bis(imidazotetrazine)s with saturated spacer groups. Jill Arrowsmith, Sharon A. Jennings, David A. F. Langnel, Richard T. Wheelhouse, Malcolm F. G. Stevens
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 4432
- A new route to the antitumour drug temozolomide, but not
thiotemozolomide. Yongfeng Wang, Philip R. Lowe, William T. Thomson, Jonathan Clark, Malcolm F. G. Stevens
, Chem. Commun.
, 1997
, 363
- Antitumour imidazotetrazines. Part 36.1 Conversion of 5-aminoimidazole-4-carboxamide to imidazo[5,1-d ][1,2,3,5]tetrazin-4(3H )-ones and imidazo[1,5-a][1,3,5]triazin-4(3H )-ones related in structure to the antitumour agents temozolomide and mitozolomide. Yongfeng Wang, Richard T. Wheelhouse, Linxiang Zhao, David A. F. Langnel, Malcolm F. G. Stevens
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 1669