Ontology highlight
ABSTRACT:
SUBMITTER: Guggenheim KG
PROVIDER: S-EPMC3132818 | biostudies-literature | 2011 Jul
REPOSITORIES: biostudies-literature
Guggenheim Kathryn G KG Butler Jeffrey D JD Painter Phillip P PP Lorsbach Beth A BA Tantillo Dean J DJ Kurth Mark J MJ
The Journal of organic chemistry 20110622 14
Routes to structurally unique spiro-fused pyrazolidoylisoxazolines are reported. These methods start with monosubstituted hydrazines or hydrazides and utilize the nitrile oxide 1,3-dipolar cycloaddition reaction to generate the targeted spiro-fused bis-heterocycles. Molecular shape space diversity analyses were performed on these pyrazolidoylisoxazolines showing that manipulation of the appended R groups significantly changes the molecular shape. ...[more]