Regio-, stereo-, and enantioselective synthesis of cyclobutanols by means of the photoaddition of 1,3-dioxin-4-ones and lipase-catalyzed acetylation
- 31 December 1992
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 3 (2) , 313-328
- https://doi.org/10.1016/s0957-4166(00)80211-6
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Doubts about the Libit's method for the synthesis of the "Corey" intermediate using photocycloaddition as a key step.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Synthesis of 5,6-Unsubstituted 1,3-Dioxin-4-onesSynthesis, 1985
- The chemistry of an allylsilane: The synthesis of a prostaglandin intermediate and of loganinTetrahedron, 1981
- Photochemical annelations. 6. Four-carbon photochemical annelation of alkenes with 2,2,6-trimethyl-1,3-dioxolenoneJournal of the American Chemical Society, 1980
- Regioselectivity in [π2 + π2] photocycloaddition reactions between cyclopent-2-enones and β-oxysubstituted acrylatesTetrahedron Letters, 1978
- New synthetic methods. Stereocontrolled bicycloannulation: an approach to gibberellinsThe Journal of Organic Chemistry, 1978
- A photochemical approach to the 11-deoxyprostaglandin intermediateTetrahedron Letters, 1977
- Photochemical syntheses. 37. Enone photoannelationAccounts of Chemical Research, 1971
- Photoreaction of AcetoacetateBulletin of the Chemical Society of Japan, 1970
- PHOTOCHEMICAL SYNTHESES: 6. THE FORMATION OF HEPTANDIONES FROM ACETYLACETONE AND ALKENESCanadian Journal of Chemistry, 1963