Use of Acylhydrazones as Stable Surrogates of Unstable Imines in Allylation, Mannich-Type, and Cyanide Addition Reactions-Reference-Cited by-同舟云学术

Use of Acylhydrazones as Stable Surrogates of Unstable Imines in Allylation, Mannich-Type, and Cyanide Addition Reactions

Published:1999-09-23 Issue:21 Volume:64 Page:8054-8057
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Manabe Kei¹,Oyamada Hidekazu¹,Sugita Kasumi¹,Kobayashi Shū¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, CREST, Japan Science and Technology Corporation (JST), Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo991009q

Reference19 articles.

1. Efficient Regio- and Enantioselective Mannich Reactions

2. Organocerium additions to SAMP-hydrazones: general synthesis of chiral amines

3. Enantioselective Synthesis of α-Substituted Primary Amines by Nucleophilic Addition to Aldehyde-SAMP Hydrazones

4. Organolithium addition to aldehyde dimethylhydrazones: a highly diastereocontrolled synthesis of threo 2-amino alcohols, and (1R,2R)-(-)-norpseudoephedrine

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