Direct Asymmetric a nti -Mannich-Type Reactions Catalyzed by a Designed Amino Acid
โ Scribed by Mitsumori, Susumu; Zhang, Haile; Ha-Yeon Cheong, Paul; Houk, K. N.; Tanaka, Fujie; Barbas, Carlos F.
- Book ID
- 120022621
- Publisher
- American Chemical Society
- Year
- 2006
- Tongue
- English
- Weight
- 52 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0002-7863
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๐ SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
The first (S)-2-methoxymethylpyrrolidine (SMP)-catalyzed direct asymmetric Mannich-type reactions of unmodified aldehydes with N-PMP-protected a-imino ethyl glyoxylate are described. The reaction proceeded in a highly anti-selective manner (dr up to 19:1) with enantioselectivities between 74 and 92%