Literature DB >> 21975423

Enantioselective methodologies for the synthesis of spiro compounds.

Ramon Rios1.   

Abstract

The enantioselective synthesis of spirocycles has been a long time pursued dream for organic chemists. Since the first pioneering efforts of Tamao and coworkers in the enantioselective construction of spirosilanes, many efforts have been devoted to the development of new and promising asymmetric methodologies. Remarkably, with the advent of organocatalysis the number of methodologies has been highly increased. The aim of this tutorial review is to summarize the last trends and developments reported in the literature in the enantioselective synthesis of spirocompounds. This journal is © The Royal Society of Chemistry 2012

Entities:  

Year:  2011        PMID: 21975423     DOI: 10.1039/c1cs15156h

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  32 in total

1.  Synthesis of Spirocyclic Ethers by Enantioselective Copper-Catalyzed Carboetherification of Alkenols.

Authors:  Shuklendu D Karyakarte; Chanchamnan Um; Ilyas A Berhane; Sherry R Chemler
Journal:  Angew Chem Int Ed Engl       Date:  2018-09-03       Impact factor: 15.336

Review 2.  Recent developments in green approaches for sustainable synthesis of indole-derived scaffolds.

Authors:  Shima Nasri; Mohammad Bayat; Fatemeh Rostami Miankooshki; Narges Habibi Samet
Journal:  Mol Divers       Date:  2022-01-15       Impact factor: 2.943

3.  Asymmetric Synthesis of All-Carbon Quaternary Spirocycles via a Catalytic Enantioselective Allylic Alkylation Strategy.

Authors:  Samantha E Shockley; J Caleb Hethcox; Brian M Stoltz
Journal:  Tetrahedron Lett       Date:  2017-07-05       Impact factor: 2.415

Review 4.  Therapeutic Potential of Spirooxindoles as Antiviral Agents.

Authors:  Na Ye; Haiying Chen; Eric A Wold; Pei-Yong Shi; Jia Zhou
Journal:  ACS Infect Dis       Date:  2016-05-05       Impact factor: 5.084

5.  Enantioselective cyclization of enamide-ynes and application to the synthesis of the kopsifoline core.

Authors:  Britton K Corkey; Stephen T Heller; Yi-Ming Wang; F Dean Toste
Journal:  Tetrahedron       Date:  2013-07-08       Impact factor: 2.457

6.  Synthesis of a family of spirocyclic scaffolds: building blocks for the exploration of chemical space.

Authors:  Sarvesh Kumar; Paul D Thornton; Thomas O Painter; Prashi Jain; Jared Downard; Justin T Douglas; Conrad Santini
Journal:  J Org Chem       Date:  2013-06-26       Impact factor: 4.354

7.  Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols.

Authors:  Thomas O Painter; Jonathon R Bunn; Frank J Schoenen; Justin T Douglas; Victor W Day; Conrad Santini
Journal:  J Org Chem       Date:  2013-04-01       Impact factor: 4.354

8.  Streocontrolled construction of six vicinal stereogenic centers on spiropyrazolones via organocascade Michael/Michael/1,2-addition reactions.

Authors:  Pankaj Chauhan; Suruchi Mahajan; Charles C J Loh; Gerhard Raabe; Dieter Enders
Journal:  Org Lett       Date:  2014-05-19       Impact factor: 6.005

9.  Unexpected Substituent Effects in Spiro-Compound Formation: Steering N-Aryl Propynamides and DMSO toward Site-Specific Sulfination in Quinolin-2-ones or Spiro[4,5]trienones.

Authors:  Xiaoxian Li; Yuanxun Wang; Yaxin Ouyang; Zhenyang Yu; Beibei Zhang; Jingran Zhang; Haofeng Shi; Han Zuilhof; Yunfei Du
Journal:  J Org Chem       Date:  2021-06-29       Impact factor: 4.354

10.  Cross-trienamines in asymmetric organocatalysis.

Authors:  Kim Søholm Halskov; Tore Kiilerich Johansen; Rebecca L Davis; Marianne Steurer; Frank Jensen; Karl Anker Jørgensen
Journal:  J Am Chem Soc       Date:  2012-07-30       Impact factor: 15.419

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