Calixarene and resorcinarene macrocycles are renowned for their ability to form inclusion
complexes or act as molecular scaffolds. The addition of chirality to these non-planar …

Resorcin [4] arenes are not as extensively studied as their sister compounds, calix [4]
arenes, owing to challenges in synthetic methodologies for their derivatization from the …

The regioselective reaction of resorcarene octaols 1 with 4 equiv of arylsulfonyl chlorides
and Et3N in MeCN gives in 30− 60% yield the C 2v symmetrical tetrasulfonates 3. The mild …

Reversed‐phase high‐performance liquid chromatography [LiChrosorb RP‐18, UV
detection at 254 nm and acetonitrile‐water (86: 14, v/v) as mobile phase] was applied to …

The regioselective condensation of resorcarene tetratosylates 3/4 with formaldehyde and
various primary amines readily gives bis-benzoxazines 5/6 in 65− 86% yield. The chiral, C 2 …

Lewis acids catalyse the condensation of isovaleraldehyde with 1, 3-dimethoxybenzene. All
conformers formed in this reaction were isolated and analysed spectroscopically. SnCl4 …

The enantioselective addition of diethylzinc to benzaldehyde catalysed by a range of chiral
bridged resorcinarenes has been studied, and the results used as a means of probing …

A study towards a convergent synthesis of sulfonimide-type dendrons and dendrimers was
undertaken. Dendrons up to the third-generation bearing chlorosulfo-groups at their focal …

Two novel multifunctional initiators for atom transfer radical polymerization (ATRP) were
synthesized by derivatization of tetraethylresorcinarene. The derivatization induced a …

Selective derivatisation of resorcinarene ethers via an ortholithiation approach - RSC Advances
(RSC Publishing) DOI:10.1039/C3RA00141E Royal Society of Chemistry View PDF …