Preprint Review Version 1 This version is not peer-reviewed

Metal Catalyzed Suzuki-Miyaura Cross-Coupling– Efficient Methodology for Synthesis the Natural and non-Natural biological active Molecules

Version 1 : Received: 15 May 2017 / Approved: 15 May 2017 / Online: 15 May 2017 (18:30:52 CEST)

How to cite: Israr, H.; Kaousar, S.; Rasool, N.; Ahmad, G.; Aziz, M.N.M.; Akhtar, M.N.; Alitheen, N.B. Metal Catalyzed Suzuki-Miyaura Cross-Coupling– Efficient Methodology for Synthesis the Natural and non-Natural biological active Molecules. Preprints 2017, 2017050115 (doi: 10.20944/preprints201705.0115.v1). Israr, H.; Kaousar, S.; Rasool, N.; Ahmad, G.; Aziz, M.N.M.; Akhtar, M.N.; Alitheen, N.B. Metal Catalyzed Suzuki-Miyaura Cross-Coupling– Efficient Methodology for Synthesis the Natural and non-Natural biological active Molecules. Preprints 2017, 2017050115 (doi: 10.20944/preprints201705.0115.v1).

Abstract

New class of biologically active and non-active compounds can be synthesized via transition metal mediated Suzuki cross coupling reaction that has a great impact on the advancement of organic chemistry. These resulted products can lend a helping hand in pharmaceutical and polymer chemistry for the betterment of mankind. Suzuki-Miyaura cross coupling reaction is one of the best tools through which many natural and non-natural compounds can be synthesized.

Subject Areas

Palladium; Suzuki cross coupling; natural product; non-natural product

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