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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 10, 1980 - Issue 5
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Original Articles

Pinacol-Type Rearrangements of 1, 2-Epoxy-9-Decalols

James A. Marshall Department of Chemistry, Northwestern University Evanston, Illinois, 60201, U.S.A.
&
James A. Kerschen Department of Chemistry, Northwestern University Evanston, Illinois, 60201, U.S.A.
Pages 409-414 | Published online: 05 Dec 2006

Citations (6)

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Read on this site (1)

Göran Magnusson. (1990) REARRANGEMENTS OF EPOXY ALCOHOLS AND RELATED COMPOUNDS. A REVIEW. Organic Preparations and Procedures International 22:5, pages 547-574.
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Articles from other publishers (5)

Bingfeng Sun & Xingxiang Xu. (2006) Stereospecific rearrangement of α-hydroxyepoxide: efficient approach to the trans-bicyclo[9.3.0]tetradecane core en route to clavulactone. Tetrahedron Letters 47:3, pages 299-302.
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M. Bartóak. 1993. Hydroxyl, Ether and Peroxide Groups (1993). Hydroxyl, Ether and Peroxide Groups (1993) 843 903 .
Charles M. Marson, Steven Harper, Andrew J. Walker, Jane Pickering, Jonathan Campbell, Roger Wrigglesworth & Simon J. Edge. (1993) Lewis acid mediated reactions of 2,3-epoxyalcohols: an efficient stereocontrolled route to polycyclic diols. Tetrahedron 49:45, pages 10339-10354.
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Bruce Rickborn. 1991. Comprehensive Organic Synthesis. Comprehensive Organic Synthesis 733 775 .
J. A. MARSHALL & J. A. KERSCHEN. (1980) ChemInform Abstract: PINACOL-TYPE REARRANGEMENTS OF 1,2-EPOXY-9-DECALOLS. Chemischer Informationsdienst 11:37.
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