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Solution- and solid-phase asymmetric synthesis of substituted N-hydroxypyrrolidine dicarboxylic acids

✍ Scribed by Stephen Hanessian; Malken Bayrakdarian


Book ID
104252445
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
309 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


Nitrone ylids prepared from a-amino aldehyde derivatives undergo 1,3-dipolar cyclocondensation reactions to give enantiopure C-4 branched N-hydroxy proline esters. The different functional groups can be manipulated to provide diversely substituted N-hydroxypyrrolidine dicarboxylic acids. The reaction can be adapted to solid-phase synthesis.


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