𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Regioselective openings of 2,3-epoxy acids with organocuprates

✍ Scribed by J.Michael Chong; K.Barry Sharpless


Book ID
104226839
Publisher
Elsevier Science
Year
1985
Tongue
French
Weight
227 KB
Volume
26
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Lithium organocuprates react with 3-alkyl-2,3-epoxy acids (glycidic acids) to afford the products of ring-opening in good yield.

The regiochemistry of ringopening is dependent on the stereochemistry of the epoxy acid.


πŸ“œ SIMILAR VOLUMES


Regioselective titanium mediated reducti
✍ Li-xin Dai; Bo-liang Lou; Ying-zhi Zhang; Guang-zhong Guo πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 French βš– 191 KB

Lithium borohydride reduction of 2,3-epoxy alcohols was shown to yield 1,2-diols in high regioselectivity with the aid of titanium tetraisopropoxide in benzene solution.

ChemInform Abstract: Regioselective Ring
✍ T. HONDA; H. MIZUTANI πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 36 KB πŸ‘ 1 views

## 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 β€œFull Text” option. The original article is trackable v