Literature DB >> 29920922

Design and Synthesis of Polycycles, Heterocycles, and Macrocycles via Strategic Utilization of Ring-Closing Metathesis.

Sambasivarao Kotha1, Milind Meshram1, Yuvaraj Dommaraju1.   

Abstract

In this perspective, we summarize new synthetic approaches for the construction of various polycyclic compounds involving ring-closing metathesis as a key step. In this regard, we used ring-closing metathesis in combination with other popular reactions like Suzuki-Miyaura coupling, Claisen rearrangement, Fischer indolization, Grignard addition, Diels-Alder reaction, and [2+2] cycloaddition reaction etc. To this end, a variety of functional molecules such as α-amino acids, cyclophanes, heterocycles, propellanes, spirocycles, and macrocycles have been prepared. The strategies developed and the molecules prepared here play a key role in designing new materials and also act as lead compounds in drug design. The strategies and tactics developed here are useful to design polycycles, macrocycles, and heterocycles of diverse ring systems.
© 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Ring-closing metathesis; cyclophanes; heterocycles; polycycles; propellanes; spirocycles; α-amino acids

Year:  2018        PMID: 29920922     DOI: 10.1002/tcr.201800025

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  2 in total

1.  Advanced sol-gel process for efficient heterogeneous ring-closing metathesis.

Authors:  Shiran Aharon; Dan Meyerstein; Eyal Tzur; Dror Shamir; Yael Albo; Ariela Burg
Journal:  Sci Rep       Date:  2021-06-15       Impact factor: 4.379

2.  Application of New Efficient Hoveyda-Grubbs Catalysts Comprising an N→Ru Coordinate Bond in a Six-Membered Ring for the Synthesis of Natural Product-Like Cyclopenta[b]furo[2,3-c]pyrroles.

Authors:  Alexandra S Antonova; Marina A Vinokurova; Pavel A Kumandin; Natalia L Merkulova; Anna A Sinelshchikova; Mikhail S Grigoriev; Roman A Novikov; Vladimir V Kouznetsov; Kirill B Polyanskii; Fedor I Zubkov
Journal:  Molecules       Date:  2020-11-17       Impact factor: 4.411

  2 in total

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