Literature DB >> 21892505

New synthesis of spirocycles by utilizing in situ forming hypervalent iodine species.

Toshifumi Dohi1, Tomofumi Nakae, Yohei Ishikado, Daishi Kato, Yasuyuki Kita.   

Abstract

A very effective spirocyclization procedure for installing nucleophiles (Nu = N(3), NO(2), SCN, SO(2)Tol, and halogens) via iodonium(III) salts has been developed using the combination of iodoarene and mCPBA. The high-yielding syntheses of the cyclohexadienone-type spirocyclic compounds 2 having varied functionalities in the skeletons have been achieved from the aryl alkynes 1 with the optimized bis(iodoarene) 3h.

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Year:  2011        PMID: 21892505     DOI: 10.1039/c1ob06199b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  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

2.  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

3.  One-Pot C-H Functionalization of Arenes by Diaryliodonium Salts.

Authors:  Marcus Reitti; Piret Villo; Berit Olofsson
Journal:  Angew Chem Int Ed Engl       Date:  2016-06-08       Impact factor: 15.336

Review 4.  Synthesis of spirocyclic scaffolds using hypervalent iodine reagents.

Authors:  Fateh V Singh; Priyanka B Kole; Saeesh R Mangaonkar; Samata E Shetgaonkar
Journal:  Beilstein J Org Chem       Date:  2018-07-17       Impact factor: 2.883

  4 in total

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