Highly diastereoselective synthesis of (6-methylenepyrrolo[1,2-c]oxazol- 7-yl)-methylphosphonate by an application of radical reaction

Article abstract of DOI:10.1080/00397919908085991

Highly diastereoselective synthesis of (6-methylenepyrrolo[1,2-c]- oxazol-7-yl)methylphosphonate 5 was achieved by an application of intramolecular radical cyclization of vinyl radical to β-carbon of unsaturated phosphonate.

Full text of DOI:10.1080/00397919908085991

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Highly Diastereoselective Synthesis of
(6-Methylenepyrrolo [1,2-C] oxazol-7-
yl)methylphosphonate by an Application of Radical
Reaction
Yoko Yuasa , Nobuko Fujimaki , Tsutomu Yokomatsu , Jun Ando & Shiroshi
Shibuya
To cite this article: Yoko Yuasa , Nobuko Fujimaki , Tsutomu Yokomatsu , Jun Ando & Shiroshi
Shibuya (1999) Highly Diastereoselective Synthesis of (6-Methylenepyrrolo [1,2-C] oxazol-7-
yl)methylphosphonate by an Application of Radical Reaction, Synthetic Communications, 29:20,
3573-3580, DOI: 10.1080/00397919908085991
To link to this article: http://dx.doi.org/10.1080/00397919908085991
Published online: 17 Sep 2007.
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Date: 09 June 2016, At: 14:11