Enantioselective, Stereodivergent Hydroazidation and Hydroamination of Allenes Catalyzed by Acyclic Diaminocarbene (ADC) Gold(I) Complexes-Reference-Cited by-同舟云学术

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Enantioselective, Stereodivergent Hydroazidation and Hydroamination of Allenes Catalyzed by Acyclic Diaminocarbene (ADC) Gold(I) Complexes

Published:2016-04-20 Issue:20 Volume:128 Page:6183-6187
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Khrakovsky Dimitri A.¹,Tao Chuanzhou¹²,Johnson Miles W.¹³,Thornbury Richard T.¹,Shevick Sophia L.¹,Toste F. Dean¹

Affiliation:

1. Department of Chemistry University of California, Berkeley Berkeley CA 94720 USA

2. School of Chemical Engineering Huaihai Institute of Technology Lianyungang 222005 P.R. China

3. Division of Chemistry and Chemical Engineering California Institute of Technology Pasadena CA 91125 USA

Funder

NIH

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201601550

Reference81 articles.

1. Applications of allylamines for the syntheses of aza-heterocycles

2. Sterically Biased 3,3-Sigmatropic Rearrangement of Azides: Efficient Preparation of Nonracemic α-Amino Acids and Heterocycles

3. On the flexibility of allylic azides as synthetic intermediates

4. For selected examples see:

5. A Short Synthetic Approach to Chiral Serine Azido Derivatives

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2. Transition-metal acyclic carbene complexes: building blocks for luminescent, stimuli-responsive, bioactive materials and catalysts;Materials Chemistry Frontiers;2023

3. [3,3]‐Sigmatropic Rearrangements of Naphthyl 1‐Propargyl Ethers: para ‐Propargylation and Catalytic Asymmetric Dearomatization;Angewandte Chemie;2022-11-29

4. [3,3]‐Sigmatropic Rearrangements of Naphthyl 1‐Propargyl Ethers: para ‐Propargylation and Catalytic Asymmetric Dearomatization;Angewandte Chemie International Edition;2022-11-28

5. Chiral Ligands for Au(I), Au(III), and Au(I)/Au(III) Redox Catalysis;Israel Journal of Chemistry;2022-08-29

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