CamTHP*OH: a camphor-derived delta-lactol auxiliary for the effective desymmetrization of attached glycinamide residues. Asymmetric synthesis of alpha-amino carbonyl compounds.
Stereoselective allylation of camphor and subsequent terminal hydroformylation affords a new delta-lactol auxiliary (camTHP*OH) on multigram scale. Stereoselective condensation with glycine dimethylamide and Cbz protection affords a camTHP*-desymmetrized glycinamide building block which undergoes ef...
Päätekijät: | Dixon, D, Horan, R, Monck, N |
---|---|
Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2004
|
Samankaltaisia teoksia
-
Highly stereoselective Michael addition reactions of CamTHP*-desymmetrized glycinamide for the synthesis of functionally dense amino acid derivatives.
Tekijä: Dixon, D, et al.
Julkaistu: (2004) -
6-methyl delta-lactol derived chiral glycine equivalents for the asymmetric synthesis of protected alpha-amino amides
Tekijä: Dixon, D, et al.
Julkaistu: (2004) -
Allylation of lactol in water
Tekijä: Zheng, Mengxue, et al.
Julkaistu: (2025) -
N-Acryloyl glycinamide
Tekijä: Jan Seuring, et al.
Julkaistu: (2011-08-01) -
ORGN 134-Desymmetrization of bisvinyltriflates via palladium-catalyzed carbonylation
Tekijä: Byrne, S, et al.
Julkaistu: (2006)