A Trial toward the Synthesis of γ-Fluorinated β-Amino-α-thiohydroxyamino Acid: A Finding of Desulfurizative C−C Bond Formation in Thio-Wittig-Type Rearrangement of S-(N-Aryltrifluoroacetimidoyl)thioglycolates-Reference-Cited by-同舟云学术

A Trial toward the Synthesis of γ-Fluorinated β-Amino-α-thiohydroxyamino Acid: A Finding of Desulfurizative C−C Bond Formation in Thio-Wittig-Type Rearrangement of S-(N-Aryltrifluoroacetimidoyl)thioglycolates

Published:2001-01-06 Issue:3 Volume:66 Page:1026-1029
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Uneyama Kenji¹,Ohkura Hironari¹,Hao Jian¹,Amii Hideki¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Engineering, Okayama University, Okayama 700-8530, Japan uneyamak@cc.okayama-u.ac.jp

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0010330

Reference29 articles.

1. Selectfluor™ reagent F-TEDA-BF4 in action: tamed fluorine at your service

2. Perfluoroalkylation with Organosilicon Reagents

3. Enantioselective Biomimetic Transamination of β-Keto Carboxylic Acid Derivatives. An Efficient Asymmetric Synthesis of β-(Fluoroalkyl) β-Amino Acids

4. First Highly Diastereoselective Synthesis of syn α-Methyl β-Fluoroalkyl β-Amino Esters

5. New Strategies for the Synthesis of Fluorinated Vinylogous Amidines and β-Enamino Ketones

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