Solid phase synthesis of 17α-E/Z-(X-phenyl)-vinyl estradiols using the stille coupling reaction

Choon Young Lee, Robert N. Hanson

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

As a continuation of our program to develop probes for the hormone binding domain (HBD) of the estrogen receptor (ER), we designed a series of novel 17α-E/Z-(X-phenyl)-vinyl estradiols. Based upon our experience with solution chemistry we applied solid phase synthesis using carboxylated resins to synthesize the new compounds. The Stille coupling reaction permitted the introduction of a variety of functional groups and positional isomers on the terminal phenyl group. Subsequent cleavage from the resin generated a series of novel estradiol derivatives.

Original languageEnglish
Pages (from-to)1623-1629
Number of pages7
JournalTetrahedron
Volume56
Issue number12
DOIs
StatePublished - Mar 17 2000

Keywords

  • Carboxylation
  • Estrogen receptor probes
  • Hydrostannylation
  • Solid phase synthesis
  • Stille reaction

Fingerprint

Dive into the research topics of 'Solid phase synthesis of 17α-E/Z-(X-phenyl)-vinyl estradiols using the stille coupling reaction'. Together they form a unique fingerprint.

Cite this