Literature DB >> 28960012

Nazarov reaction: current trends and recent advances in the synthesis of natural compounds and their analogs.

Maxim G Vinogradov1, Olga V Turova, Sergei G Zlotin.   

Abstract

The Nazarov reaction (cyclization) is one of the most useful synthetic tools for the stereoselective preparation of various cyclopentenone scaffolds. This review summarizes recent applications of this reaction to the synthesis of natural compounds and their usefulness to pharmacology analogs published over 2005-2016. Modern protocols for the facile generation of key cationic intermediates and efficient catalytic, in particular asymmetric, versions of Nazarov cyclization are considered. Available literature data are for the first time classified according to the chemical structures of the products, which include relatively simple non-annulated functionalized cyclopentenoids and complex polynuclear cyclopentenone derivatives annulated with one or more non-aromatic, aromatic or heteroaromatic rings. This classification is convenient for specialists in organic synthesis and for researchers working in the area of medicinal and biomolecular chemistry.

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Year:  2017        PMID: 28960012     DOI: 10.1039/c7ob01981e

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


  8 in total

1.  Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination.

Authors:  Joshua R Corbin; Devin R Ketelboeter; Israel Fernández; Jennifer M Schomaker
Journal:  J Am Chem Soc       Date:  2020-03-10       Impact factor: 15.419

2.  Synthetic Studies toward the Hamigerans with a 6-7-5 Tricyclic Core.

Authors:  Baiyang Jiang; Mingji Dai
Journal:  Org Lett       Date:  2020-05-13       Impact factor: 6.005

3.  Ti-Catalyzed and -Mediated Oxidative Amination Reactions.

Authors:  Ian A Tonks
Journal:  Acc Chem Res       Date:  2021-08-22       Impact factor: 24.466

4.  Electrochemically Mediated Oxidation of Sensitive Propargylic Benzylic Alcohols.

Authors:  Chad E Hatch; Maxwell I Martin; Philip H Gilmartin; Lu Xiong; Danielle J Beam; Glenn P A Yap; Matthew J Von Bargen; Joel Rosenthal; William J Chain
Journal:  Org Lett       Date:  2022-02-11       Impact factor: 6.072

5.  Enyne diketones as substrate in asymmetric Nazarov cyclization for construction of chiral allene cyclopentenones.

Authors:  Shengbiao Tang; Peng Zhang; Ying Shao; Jiangtao Sun
Journal:  Nat Commun       Date:  2022-06-07       Impact factor: 17.694

6.  Mechanism of Ti-Catalyzed Oxidative Nitrene Transfer in [2 + 2 + 1] Pyrrole Synthesis from Alkynes and Azobenzene.

Authors:  Zachary W Davis-Gilbert; Xuelan Wen; Jason D Goodpaster; Ian A Tonks
Journal:  J Am Chem Soc       Date:  2018-05-31       Impact factor: 15.419

7.  Optimization of Nazarov Cyclization of 2,4-Dimethyl-1,5-diphenylpenta-1,4-dien-3-one in Deep Eutectic Solvents by a Design of Experiments Approach.

Authors:  Stefano Nejrotti; Alberto Mannu; Marco Blangetti; Salvatore Baldino; Andrea Fin; Cristina Prandi
Journal:  Molecules       Date:  2020-12-04       Impact factor: 4.411

8.  Total synthesis of endiandric acid J and beilcyclone A from cyclooctatetraene.

Authors:  Oussama Yahiaoui; Adrian Almass; Thomas Fallon
Journal:  Chem Sci       Date:  2020-07-29       Impact factor: 9.825

  8 in total

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