Reduction of N-Allylamides by LiAlH4: Unexpected Attack of the Double Bond with Mechanistic Studies of Product and Byproduct Formation-Reference-Cited by-同舟云学术

Reduction of N-Allylamides by LiAlH4: Unexpected Attack of the Double Bond with Mechanistic Studies of Product and Byproduct Formation

Published:2014-10-27 Issue:21 Volume:79 Page:10284-10295
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Thiedemann Birk¹,Schmitz Christin M. L.¹,Staubitz Anne¹

Affiliation:

1. Otto-Diels-Institute for Organic Chemistry, University of Kiel, Otto-Hahn-Platz 4, 24098 Kiel, Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo501907v

Reference59 articles.

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2. Synthesis of cytosinine, the nucleoside component of antibiotic blasticidin S

3. THE ABSOLUTE STRUCTURE OF ORYZOXYMYCIN

4. THE STRUCTURES OF ORYZOXYMYCIN AND ITS DIMERIZATION PRODUCT

5. Shikimate-derived metabolites. 10. Synthetic studies on the biosynthesis of para-aminobenzoic acid.

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