Synlett 2009(10): 1690-1691  
DOI: 10.1055/s-0029-1217323
SPOTLIGHT
© Georg Thieme Verlag Stuttgart ˙ New York

Simmons-Smith Reagent (Et2Zn, CH2I2): An Efficient Reagent in Organic Synthesis

Ali Maleki*
Department of Chemistry, Shahid Beheshti University, P.O. Box 19396-4716, Tehran, Iran
e-Mail: a_maleki@sbu.ac.ir;
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Publikationsverlauf

Publikationsdatum:
02. Juni 2009 (online)

Introduction

The diethylzinc/diiodomethane or zinc-diiodomethane (Et2Zn, CH2I2 or Zn, CH2I2 = ICH2ZnI) known as Simmons-Smith reagent is probably the best known carbenoid reagent in organic syntheses. [¹] This ether soluble reagent has been used mainly for the conversion of al­kenes into cyclopropanes [¹] via stereospecific and supra­facial CH2 addition using chiral auxiliaries, [²] reagents [³] and catalysts. [4]

Due to the presence of cyclopropanes in many biologically and medicinally important molecules, [5] natural products, [6] essential oils [7] and the marine cyanobacteriums, [8] some recent applications of Simmons-Smith reagent are reported herein.