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- [1] SYNTHESIS OF THE OPTICALLY-ACTIVE FORMS OF 4,10-DIHYDROXY-1,7-DIOXASPIRO[5.5]UNDECANE AND THEIR CONVERSION TO THE ENANTIOMERS OF 1,7-DIOXASPIRO[5.5]UNDECANE, THE OLIVE FLY PHEROMONETETRAHEDRON, 1985, 41 (13) : 2751 - 2758MORI, KUEMATSU, TYANAGI, KMINOBE, M
- [2] SYNTHESIS OF THE ENANTIOMERS OF 1,7-DIOXASPIRO[5.5]UNDECANE AND 4-HYDROXY 1,7-DIOXASPIRO[5.5]UNDECANE, THE COMPONENTS OF THE OLIVE FLY PHEROMONETETRAHEDRON LETTERS, 1984, 25 (35) : 3875 - 3878MORI, KUEMATSU, TWATANABE, HYANAGI, KMINOBE, M
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- [5] SYNTHESIS OF 2,8-SUBSTITUTED 1,7-DIOXASPIRO[5.5]UNDECANES AND 1,4,7,10-TETRAOXASPIRO[5.5]UNDECANES BY AN OXYAMINATION REACTIONSYNLETT, 1990, (10) : 615 - 616LEMAIRE, MGOURCY, JGDAUPHIN, GJEMINET, G
- [6] ISOLATION AND SYNTHESIS OF 3-HYDROXY-1 AND 4-HYDROXY-1,7-DIOXASPIRO[5.5]UNDECANES FROM THE OLIVE FLY (DACUS-OLEAE)JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (11) : 601 - 603BAKER, RHERBERT, RHPARTON, AH
- [7] HYDROXY-FUNCTIONALIZED CONJUGATED NITROOLEFINS AS IMMEDIATE PRECURSORS OF SPIROKETALS - A NEW SYNTHESIS OF 1,7-DIOXASPIRO[5.5]UNDECANE AND (E)-2-METHYL-1,7-DIOXASPIRO[5.6]DODECANEJOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (23): : 3159 - 3160BALLINI, RPETRINI, M
- [8] Claisen self-condensation/decarboxylation as the key steps in the synthesis of C2-symmetrical 1,7-dioxaspiro[5.5]undecanesTETRAHEDRON LETTERS, 2005, 46 (37) : 6195 - 6198Lastdrager, BTimmer, MSMvan der Marel, GAOverkleeft, HS
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- [10] NITRO KETONES IN ORGANIC-SYNTHESIS - A NEW, SHORT SYNTHESIS OF RACEMIC TRANS-2-METHYL-1,7-DIOXASPIRO[5.5]UNDECANE, TRANS,TRANS AND TRANS,CIS-2,8-DIMETHYL-1,7-DIOXASPIRO[5.5]UNDECANE BY HENRY REACTIONLIEBIGS ANNALEN DER CHEMIE, 1994, (12): : 1235 - 1237BALLINI, RBOSICA, GSCHAAFSTRA, R