α-Sulfonyl Radical Initiated Intramolecular Tandem Radical Cyclization: Stereochemistries of a Pair of Doubly Cyclized Products

Lindsay Byrne, M. Phomakotr, C. Poolsanong, V. Reutrakul, Brian Skelton, Allan White

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Room-temperature single-crystal X-ray structure determinations are recorded for trans-1,2,3,3a,9,9a-Hexahydro-cyclopenta[b]-1-benzothiapyran-4,4-dioxide and its 3a-methyl analogue, minor products of the α-sulfonyl radical-initiated intramolecular tandem radical cyclization of H2C=CH(CH2)CRBrSO2Ph (R = H, CH3), confirming the assigned structures and rigorously establishing the trans relationship at the ring junctions.
Original languageEnglish
Pages (from-to)715-717
JournalAustralian Journal of Chemistry
Volume56
Issue number7
DOIs
Publication statusPublished - 2003

Fingerprint

Dive into the research topics of 'α-Sulfonyl Radical Initiated Intramolecular Tandem Radical Cyclization: Stereochemistries of a Pair of Doubly Cyclized Products'. Together they form a unique fingerprint.

Cite this