Thiacalix[4] arenes with terminal thiol groups at the lower rim: Synthesis and structure

Methods were developed for the synthesis of ω-mercaptoalkoxy derivatives of thiacalix[4]-arenes in the 1,3-alternate conformation containing different numbers (2-5) of methylene spacers at the lower rim. The hydrazinolysis of the corresponding thioacetates is the most efficient method for the synthesis of these compounds. © 2009 Springer Science+Business Media, Inc

Thiacalix[4] arenes with terminal thiol groups at the lower rim: Synthesis and structure

Methods were developed for the synthesis of ω-mercaptoalkoxy derivatives of thiacalix[4]-arenes in the 1,3-alternate conformation containing different numbers (2-5) of methylene spacers at the lower rim. The hydrazinolysis of the corresponding thioacetates is the most efficient method for the synthesis of these compounds. © 2009 Springer Science+Business Media, Inc

Thiacalix[4] arenes with terminal thiol groups at the lower rim: Synthesis and structure

Methods were developed for the synthesis of ω-mercaptoalkoxy derivatives of thiacalix[4]-arenes in the 1,3-alternate conformation containing different numbers (2-5) of methylene spacers at the lower rim. The hydrazinolysis of the corresponding thioacetates is the most efficient method for the synthesis of these compounds. © 2009 Springer Science+Business Media, Inc

Thiacalix[4] arenes with terminal thiol groups at the lower rim: Synthesis and structure

Methods were developed for the synthesis of ω-mercaptoalkoxy derivatives of thiacalix[4]-arenes in the 1,3-alternate conformation containing different numbers (2-5) of methylene spacers at the lower rim. The hydrazinolysis of the corresponding thioacetates is the most efficient method for the synthesis of these compounds. © 2009 Springer Science+Business Media, Inc