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Results: 1-4 |
Results: 4
Trapping highly reactive dipolarophiles. Exploiting the mechanism associated with the azomethine ylide strategy for beta-lactam synthesis
Authors: Brown, GA Anderson, KM Large, JM Planchenault, D Urban, D Hales, NJ Gallagher, T
Citation: Ga. Brown et al., Trapping highly reactive dipolarophiles. Exploiting the mechanism associated with the azomethine ylide strategy for beta-lactam synthesis, J CHEM S P1, (16), 2001, pp. 1897-1900
Efficient tin hydride-mediated radical cyclisation of secondary amides. Part 1. Synthesis of a variety of substituted pyrrolidinones
Authors: Bryans, JS Large, JM Parsons, AF
Citation: Js. Bryans et al., Efficient tin hydride-mediated radical cyclisation of secondary amides. Part 1. Synthesis of a variety of substituted pyrrolidinones, J CHEM S P1, (20), 1999, pp. 2897-2904
Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis ofaromatic kainic acid analogues
Authors: Bryans, JS Large, JM Parsons, AF
Citation: Js. Bryans et al., Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis ofaromatic kainic acid analogues, J CHEM S P1, (20), 1999, pp. 2905-2910
Efficient radical cyclisation of secondary amides: An enantioselective synthesis of phenyl allokainoid
Authors: Bryans, JS Large, JM Parsons, AF
Citation: Js. Bryans et al., Efficient radical cyclisation of secondary amides: An enantioselective synthesis of phenyl allokainoid, TETRAHEDR L, 40(17), 1999, pp. 3487-3490
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