An efficient in situ reduction and cyclization reaction for synthesis of spiro compound derivatives in Fe-H2 O-AcOH medium from nitro compounds-Reference-Cited by-同舟云学术

An efficient in situ reduction and cyclization reaction for synthesis of spiro compound derivatives in Fe-H2 O-AcOH medium from nitro compounds

Published:2018-11-19 Issue:1 Volume:33 Page:e4653
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Appl Organometal Chem

Author:

Xu Hui¹,Pan Zhengbing¹,Dai Lei¹,Mao Kaimin¹,Rong Liangce¹^ORCID

Affiliation:

1. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, School of Chemistry and Materials Science; Jiangsu Normal University; Xuzhou 221116 Jiangsu China

Funder

National Natural Science Foundation of China

TAPP

Natural Science Foundation of the Jiangsu Higher Education Institutions of China

Open Foundation of Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/aoc.4653/fullpdf

Reference39 articles.

1. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

2. Catalytic Asymmetric Synthesis of Quaternary Carbon Centers. Exploratory Investigations of Intramolecular Heck Reactions of (E)-α,β-Unsaturated 2-Haloanilides and Analogues To Form Enantioenriched Spirocyclic Products

3. The Asymmetric Total Synthesis of (+)- and (−)-Spirotryprostatin B

4. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

5. Strategies for the enantioselective synthesis of spirooxindoles

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