The reactions of enolizable carbonyl compounds with azomethine functions, usually referred to as Mannich-type reactions (also termed aza ± aldol reactions), result in the formation of b-amino acids, ketones, or aldehydes. [1] These reactions are conceptually equivalent to the aldol reactions, but, i
ChemInform Abstract: α-Oxymethyl Ketone Enolates for the Asymmetric Mannich Reaction. From Acetylene and N-Alkoxycarbonylimines to β-Amino Acids.
✍ Scribed by Claudio Palomo; Mikel Oiarbide; M. Concepcion Gonzalez-Rego; Arun K. Sharma; Jesus M. Garcia; Alberto Gonzalez; Cristina Landa; Anthony Linden
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v