Biomimetic Reductive Amination of Fluoro Aldehydes and Ketones via [1,3]-Proton Shift Reaction.1 Scope and Limitations-Reference-Cited by-同舟云学术

Biomimetic Reductive Amination of Fluoro Aldehydes and Ketones via [1,3]-Proton Shift Reaction.1 Scope and Limitations

Published:1996-01-01 Issue:19 Volume:61 Page:6563-6569
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ono Taizo¹,Kukhar Valery P.¹,Soloshonok Vadim A.¹

Affiliation:

1. National Industrial Research Institute of Nagoya, Hirate-cho 1-1, Kita-ku, Nagoya City, Aichi Prefecture 462, Japan, and Institute of Bioorganic Chemistry and Petrochemistry, Ukrainian Academy of Sciences, Kiev 253160, Ukraine

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960503g

Reference38 articles.

1. A practical route to fluoroalkyl- and fluoroarylamines by base-catalyzed [1,3]-proton shift reaction

2. Cyanohydridoborate anion as a selective reducing agent

3. A convenient synthesis of hindered amines and α-trifluoromethylamines from ketones

4. Reactions of sodium borohydride in acidic media. Selective reduction of aldehydes with sodium triacetoxyborohydride

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