2009
DOI: 10.1002/chin.200915205
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Diastereoselective Synthesis of α‐Tocopherol: A New Concept for the Formation of Chromanols.

Abstract: Vitamins U 0900Diastereoselective Synthesis of α-Tocopherol: A New Concept for the Formation of Chromanols. -An alternative synthesis of α-tocopherol (V) includes 2 key steps: the first is a highly diastereoselective Shi epoxidation of alkene (II) and the second an "anti-Baldwin" epoxide ring opening under inversion of configuration. -(CHAPELAT, J.; BUSS, A.; CHOUGNET, A.; WOGGON*, W.-D.; Org. Lett. 10 (2008) 22, 5123-5126; Dep. Chem., Univ. Basel, CH-4056 Basel, Switz.; Eng.) -Bartels 15-205

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?