Use of Triethylsilane for Directed Enantioselective Reduction of Olefines: Synthesis of Pyrazino[2,1-c ][1,4]oxazine-6,9-diones with Full Control of the Absolute Configuration-Reference-Cited by-同舟云学术

Use of Triethylsilane for Directed Enantioselective Reduction of Olefines: Synthesis of Pyrazino[2,1-c ][1,4]oxazine-6,9-diones with Full Control of the Absolute Configuration

Published:2018-01-31 Issue:4 Volume:2018 Page:564-570
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Ručilová Veronika¹^ORCID,Maloň Michal²^ORCID,Soural Miroslav³^ORCID

Affiliation:

1. Department of Organic Chemistry; Faculty of Science; Palacký University; 771 46 Olomouc Czech Republic

2. JEOL Ltd.; Musashino 3-1-2, Akishima 196-8558 Tokyo Japan

3. Institute of Molecular and Translation Medicine; Faculty of Medicine and Dentistry; Palacký University; Hněvotínská 5 779 00 Olomouc Czech Republic

Funder

Ministry of Education, Youth and Sports

European Social Fund

Univerzita Palackého v Olomouci

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201701553/fullpdf

Reference55 articles.

1. Improved efficiency and selectivity in peptide synthesis: Use of triethylsilane as a carbocation scavenger in deprotection of t-butyl esters and t-butoxycarbonyl-protected sites