A facile entry to secondary cyclopropylcarbinols: Further developments in the stereospecific synthesis of (E)-homoallylic bromides

Article abstract of DOI:10.1080/00397919508013855

Cyclopropanecarboxaldehyde has been used in an improved synthesis of secondary cyclopropylcarbinols, thus allowing for further developments in the stereospecific ring opening leading to (E)-homoallylic bromides.

Full text of DOI:10.1080/00397919508013855

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Facile Entry to Secondary
Cyclopropylcarbinols
Further Developments in the
Stereospecific Synthesis of (E)-
Homoallylic Bromides
C. Ferreri a , M. Ambrosone a & C. Chatgilialoglu b
a Dipartimento di Chimica Organica e Biologica ,
Universitá di Napoli , “Federico II”, Via
Mezzocannone 16, 1-80134, Napoli, Italy
b I.Co.C.E.A., Consiglio Nazionale delle Ricerche ,
Via P. Gobetti 101, 1-40129, Bologna, Italy
Published online: 23 Sep 2006.
To cite this article: C. Ferreri , M. Ambrosone & C. Chatgilialoglu (1995) A Facile
Entry to Secondary Cyclopropylcarbinols Further Developments in the Stereospecific
Synthesis of (E)-Homoallylic Bromides, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:21, 3351-3356,
DOI: 10.1080/00397919508013855
To link to this article: http://dx.doi.org/10.1080/00397919508013855
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