Nitronate-aryne cycloaddition as a concise route to stereochemically complex fused benzisoxazolines and amino alcohols-Reference-Cited by-同舟云学术

Nitronate-aryne cycloaddition as a concise route to stereochemically complex fused benzisoxazolines and amino alcohols

Published:2023 Issue:18 Volume:21 Page:3871-3880
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Lukoyanov Alexander A.¹^ORCID,Tabolin Andrey A.¹^ORCID,Nelyubina Yulia V.²,Aksenova Svetlana A.²³,Sukhorukov Alexey Yu.¹^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991, Leninsky prospect, 47, Moscow, Russian Federation

2. A. N. Nesmeyanov Institute of Organoelement Compounds, 119991, Vavilov str. 28, Moscow, Russian Federation

3. Moscow Institute of Physics and Technology (National Research University), 141700, Institutskiy per. 9, Dolgoprudny, Moscow Region, Russian Federation

Abstract

Reaction of nitronates with arynes affords tricyclic nitroso acetals, which serve as precursors of valuable aminodiols bearing up to four contiguous stereocenters.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00235G

Reference75 articles.

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