ChemInform Abstract: Highly Enantioselective Proline-Catalyzed Direct Aldol Reaction of Chloroacetone and Aromatic Aldehydes.
✍ Scribed by Angel Martinez-Castaneda; Belen Poladura; Humberto Rodriguez-Solla; Carmen Concellon; Vicente del Amo
- Book ID
- 115552097
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 47 KB
- Volume
- 43
- 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 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract The catalytic system is excellent for direct aldol reactions of cyclic and acyclic ketones with aromatic and aliphatic aldehydes.
## Abstract The CoCl~2~/L‐proline (1:2) system was found to be an excellent catalyst for direct aldol reactions. Excellent yields (up to 93 %) and a significant improvement in diastereoselectivity (__anti__/__syn__ up to 45:1) as well as enantioselectivity (up to more than 99 % __ee__) compared wit
## 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 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 200 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