## Abstract The copper(I)‐catalyzed dipolar [2+3] cycloaddition reaction of an azide and a terminal alkyne is exploited in the preparation of various europium(III), terbium(III), and dysprosium(III) chelates (__Schemes 1–3__). By changing the nature of the alkyne and the azide, a wide range of chel
Enantioselective Synthesis of Herbarumin III by Using a Chelation-Controlled Reduction
✍ Scribed by Gowravaram Sabitha; Chitti Srinivas; Chittapragada Maruthi; Jhillu Singh Yadav
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- German
- Weight
- 163 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The total synthesis of herbarumin III (1) was achieved via an alkynide ion addition onto a chiral aldehyde and LiAlH~4~/LiI reduction as key steps (Scheme 2).
📜 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 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
## Abstract Reduction of (Z)‐β‐sulfinyl enones with NaBH~4~/ LaCl~3~·7H~2~O allows efficient access to enantiomerically pure allylic alcohols after desulfuration.