Double [3,3]-Sigmatropic Rearrangement in the Enzymatic Dioxygenation of Benzyl Azide: Preparation of Novel Synthetically Valuable Azido-diols-Reference-Cited by-同舟云学术

Double [3,3]-Sigmatropic Rearrangement in the Enzymatic Dioxygenation of Benzyl Azide: Preparation of Novel Synthetically Valuable Azido-diols

Published:2015-01-28 Issue:3 Volume:17 Page:684-687
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Thevenet Natalia¹,de la Sovera Victoria¹,Vila María Agustina¹,Veiga Nicolás¹,Gonzalez David¹,Seoane Gustavo¹,Carrera Ignacio¹

Affiliation:

1. Departamento de Química Orgánica and ‡Departamento Estrella Campos, Facultad de Química - Universidad de la República, General Flores 2124, CP 11800, Montevideo, Uruguay

Funder

Agencia Nacional de Investigaci?n e Innovaci?n, Governo do Uruguai

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol503708v

Reference23 articles.

1. Chemoenzymatic methods for the enantioselective preparation of sesquiterpenoid natural products from aromatic precursors

2. Microbial Arene Oxidations

3. Celebrating 20 Years of SYNLETT - Special Account On the Merits of Biocatalysis and the Impact of Arene cis-Dihydrodiols on Enantioselective Synthesis

4. New methods for the synthesis of certain alkaloids and terpenoids

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