The synthesis of the optically pure 1,4,5,6-tetra-O-benzyl-myo-inositols was achieved in four steps via diastereomeric 2,3-spire-acetals of myo-inositol with Land D-camphor as the key intermediates. Camphor dimethyl acetal was used for the acetalation reaction. The diastereomers were benzylated and
β¦ LIBER β¦
The absolute configuration of (+)-1,2,4,5,6-penta-O-benzyl-myo-inositol
β Scribed by R. Aneja; S. Aneja; V.P. Pathak; P.T. Ivanova
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 191 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Synthesis of the enantiomeric 1,4,5,6-te
β
Karol S. Bruzik; Grzegorz M. SalamoΕczyk
π
Article
π
1989
π
Elsevier Science
π
English
β 490 KB
The absolute configuration and optical p
β
Rajindra Aneja; Sarla G. Aneja; Alejandro Parra
π
Article
π
1995
π
Elsevier Science
π
English
β 137 KB
ChemInform Abstract: Convenient Synthesi
β
Thoniyot Praveen; Mysore S. Shashidhar
π
Article
π
2010
π
John Wiley and Sons
β 29 KB
π 2 views
ChemInform Abstract: Syntheses of Penta-
β
Shinkiti Koto; Motoko Hirooka; et al. et al.
π
Article
π
2001
π
John Wiley and Sons
β 30 KB
π 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 βFull Textβ option. The original article is trackable v
Regioselective etherification of l,2-O-i
β
Yuan Cheng-Ye; Zhai Hai-Xiao; Li Shu-Sen
π
Article
π
2010
π
John Wiley and Sons
π
English
β 503 KB
The total synthesis of (Β±)-myo-inositol-
β
S.Jane deSolms; Joseph P. Vacca; Joel R. Huff
π
Article
π
1987
π
Elsevier Science
π
French
β 201 KB