Optically active trans-4-(tert-butyldimethylsiloxymethyl)-5-(tert-butyldimethylsiloxy)-2-cyclohexenone (2) has been synthesized in 25% overall yield starting from easily available 1,4-bis(benzyloxy)-2,3-epoxy butane (3). The enone 2 reacts with excellent stereoselectivity with RCu(CN)Li thus working
β¦ LIBER β¦
Asymmetric reduction of chlorinated 4-oxopentanoates with Bakers' yeast. Synthesis of optically active .gamma.-butyrolactones and useful chiral building blocks
β Scribed by Tsuboi, Sadao; Sakamoto, Junichi; Kawano, Takayuki; Utaka, Masanori; Takeda, Akira
- Book ID
- 121480747
- Publisher
- American Chemical Society
- Year
- 1991
- Tongue
- English
- Weight
- 462 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Optically active trans-4-(tert-butyldime
β
Takeshi Hanazawa; Masakazu Koiwa; Georges P.-J. Hareau; Fumie Sato
π
Article
π
2000
π
Elsevier Science
π
French
β 116 KB
ChemInform Abstract: Optically Active tr
β
Takeshi Hanazawa; Masakazu Koiwa; Georges P.-J. Hareau; Fumie Sato
π
Article
π
2010
π
John Wiley and Sons
β 33 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