The reaction of C60 with pregnen-20-carboxaldehyde, a biologically active synthetic steroid,
by using a 1, 3-dipolar cycloaddition reaction (Prato's protocol) results in the formation of …

Novel [60] fullerene‐steroid hybrids have been synthesized by Bingel–Hirsch
cyclopropanation reaction between C60 and steroid malonates, leading to conjugates in …

The design and synthesis of fullerene–steroid hybrids by using Prato's protocol has afforded
new fullerene derivatives endowed with epiandrosterone, an important naturally occurring …

New hybrid fullerene–steroid derivatives were prepared by using the Bingel–Hirsch
protocol, by treatment of [60] fullerene with malonates bearing the appropriate steroid …

New [60] fullerene-steroid conjugates (4–6) have been synthesized by 1, 3-dipolar
cycloaddition and Bingel–Hirsch cyclopropanation reactions from suitably functionalized …

Cyclopropanations between C60 and readily available malonates bearing different steroid
moieties (4–6) by the Bingel–Hirsch protocol has allowed the synthesis of a new series of …

Cyclopropanation reactions between C60 and different malonates decorated with
monosaccharides and steroids using the Bingel‐Hirsch methodology have allowed the …

The covalently templated bis‐functionalization of C70, employing bis‐malonate 5 tethered
by an anti‐disubstituted dibenzo [18] crown‐6 (DB18C6) ether, proceeds with complete …

We report the synthesis and characterization of a fullerene‐steroid hybrid that contains H2@
C60 and a dehydroepiandrosterone moiety synthesized by a cyclopropanation reaction with …

A series of optically active cis‐3 bis‐adducts, such as (R, R, fC)‐16 (Scheme 6), was
obtained regio‐and diastereoselectively by Bingel macrocyclization of C60 with bis …