Journal article

Directed C-H Functionalization of the Adamantane Framework


Authors listHrdina, Radim

Publication year2019

Pages629-642

JournalSynthesis: Journal of Synthetic Organic Chemistry

Volume number51

Issue number3

ISSN0039-7881

eISSN1437-210X

DOI Linkhttps://doi.org/10.1055/s-0037-1610321

PublisherThieme Publishing / Georg Thieme Verlag


Abstract

This review summarizes the synthetic approaches towards 1,2-substitution pattern on the adamantane framework. Selected are the works containing the directed C-H functionalization step.

1 Introduction

2 Access to 1,2-Disubstituted Derivatives via C-H Insertion Reactions of Electrophilic Organic Species

3 Access to 1,2-Disubstituted Derivatives through Hydrogen Radical Abstraction Reactions

4 Access to 1,2-Disubstituted Derivatives Exploiting Metal-Catalyzed (Promoted) C-H Activations

5 Access to 1,2-Disubstituted Derivatives via Hydride Shift

6 Conclusion

7 Acronyms




Citation Styles

Harvard Citation styleHrdina, R. (2019) Directed C-H Functionalization of the Adamantane Framework, Synthesis: Journal of Synthetic Organic Chemistry, 51(3), Article ss-2018-z0618-sr. pp. 629-642. https://doi.org/10.1055/s-0037-1610321

APA Citation styleHrdina, R. (2019). Directed C-H Functionalization of the Adamantane Framework. Synthesis: Journal of Synthetic Organic Chemistry. 51(3), Article ss-2018-z0618-sr, 629-642. https://doi.org/10.1055/s-0037-1610321



Keywords


4,4-DISUBSTITUTED CYCLOHEXANONE ENAMINESC-H functionalizationC(SP(3))-H BONDSDELTA-CARBON ATOMFACILE SYNTHETIC ROUTESFREE-RADICAL ALKYLATIONhydride shifthydrogen abstraction reactionsinsertion reactionsSATURATED ALCOHOLSSELECTIVE FUNCTIONALIZATIONSUBSTITUTED ADAMANTANE-2,4-DIONESTRANSANNULAR CYCLIZATIONTRANSITION-STATE GEOMETRY

Last updated on 2025-02-04 at 01:10