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Synlett 1997; 1997(3): 325-326
DOI: 10.1055/s-1997-769
DOI: 10.1055/s-1997-769
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© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Combinatorial Synthesis of C(2), C(3)-Disubstituted 3-Hydroxypropionamides Utilizing Baylis-Hillman Reactions on Solid Support
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
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A four-step reaction protocol for multiple polymer-supported synthesis of structurally diverse α,β-disubstituted 3-hydroxypropionamides 10 has been developed. Variable building blocks were recruited from three monomer pools: primary/secondary amines and aryl aldehydes, the latter of which underwent incorporation into target molecules via Baylis-Hillman reactions. The potential of our approach is demonstrated by machine-assisted assemblage of a small prototype library.
multi-step solid-phase synthesis - combinatorial chemistry - Baylis-Hillman reaction - robot-assisted synthesis