ASCIDIATRIENOLIDE-A IS A 10-MEMBERED LACTONE

[1] PHENYLSELENOACETALDEHYDE, A USEFUL REAGENT FOR THE HOMOLOGATIVE CONVERSION OF HALIDES TO PHENYLSELENOMETHYL KETONES [J]. HELVETICA CHIMICA ACTA, 1979, 62 (05) : 1406 - 1410

[2] Bochkov AF, 1979, CHEM O GLYCOSIDIC BO

[3] SYNTHETIC METHODOLOGY FOR THE PREPARATION OF TRANS-2,9-DISUBSTITUTED AND CIS-2,9-DISUBSTITUTED OXONANES [J]. TETRAHEDRON LETTERS, 1989, 30 (44) : 6081 - 6084

[4] SYNTHESIS OF MEDIUM RING ETHERS .2. SYNTHESIS OF THE FULLY SATURATED CARBON SKELETON OF LAURENCIA NON-TERPENOID ETHER METABOLITES CONTAINING 7-MEMBERED, 8-MEMBERED AND 9-MEMBERED RINGS [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (01): : 83 - 94

[5] PREPARATION OF 7-MEMBERED-RING CYCLIC ETHERS AND 3-ALKYLIDENETETRAHYDROPYRANS FROM THE CYCLIZATION OF OXONIUM CATIONS DERIVED FROM UNSUBSTITUTED AND SILICON-CONTAINING 4-ALKEN-1-OLS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (24) : 5695 - 5707

[6] STUDIES TOWARDS THE SYNTHESIS OF OBTUSENYNE - A CLAISEN REARRANGEMENT APPROACH TO UNSATURATED 9-MEMBERED LACTONES [J]. TETRAHEDRON, 1991, 47 (34) : 7171 - 7178

[7] TOTAL SYNTHESIS OF THE MACROLIDE ANTIBIOTIC CYTOVARICIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (19) : 7001 - 7031

[8] ITERATIVE SYNTHESIS OF SELECTIVELY SUBSTITUTED ALPHA,BETA-UNSATURATED AND SATURATED MEDIUM-RING LACTONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (16) : 4807 - 4817

[9] CLAISEN-REARRANGEMENT-MEDIATED RING CONTRACTION OF MACROCYCLIC LACTONES - A NEW APPROACH TO CARBOCYCLES AND HETEROCYCLES [J]. TETRAHEDRON, 1986, 42 (11) : 2831 - 2846

[10] STEREOSPECIFIC DIENE SYNTHESIS USING ACETYLENE CARBOCUPRATION - PREPARATION OF NAVEL ORANGEWORM PHEROMONE AND LEUKOTRIENE ANALOGS [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1986, (10): : 1809 - 1816

[1] PHENYLSELENOACETALDEHYDE, A USEFUL REAGENT FOR THE HOMOLOGATIVE CONVERSION OF HALIDES TO PHENYLSELENOMETHYL KETONES [J]. HELVETICA CHIMICA ACTA, 1979, 62 (05) : 1406 - 1410

[2] Bochkov AF, 1979, CHEM O GLYCOSIDIC BO

[3] SYNTHETIC METHODOLOGY FOR THE PREPARATION OF TRANS-2,9-DISUBSTITUTED AND CIS-2,9-DISUBSTITUTED OXONANES [J]. TETRAHEDRON LETTERS, 1989, 30 (44) : 6081 - 6084

[4] SYNTHESIS OF MEDIUM RING ETHERS .2. SYNTHESIS OF THE FULLY SATURATED CARBON SKELETON OF LAURENCIA NON-TERPENOID ETHER METABOLITES CONTAINING 7-MEMBERED, 8-MEMBERED AND 9-MEMBERED RINGS [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1992, (01): : 83 - 94

[5] PREPARATION OF 7-MEMBERED-RING CYCLIC ETHERS AND 3-ALKYLIDENETETRAHYDROPYRANS FROM THE CYCLIZATION OF OXONIUM CATIONS DERIVED FROM UNSUBSTITUTED AND SILICON-CONTAINING 4-ALKEN-1-OLS [J]. JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (24) : 5695 - 5707

[6] STUDIES TOWARDS THE SYNTHESIS OF OBTUSENYNE - A CLAISEN REARRANGEMENT APPROACH TO UNSATURATED 9-MEMBERED LACTONES [J]. TETRAHEDRON, 1991, 47 (34) : 7171 - 7178

[7] TOTAL SYNTHESIS OF THE MACROLIDE ANTIBIOTIC CYTOVARICIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (19) : 7001 - 7031

[8] ITERATIVE SYNTHESIS OF SELECTIVELY SUBSTITUTED ALPHA,BETA-UNSATURATED AND SATURATED MEDIUM-RING LACTONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (16) : 4807 - 4817

[9] CLAISEN-REARRANGEMENT-MEDIATED RING CONTRACTION OF MACROCYCLIC LACTONES - A NEW APPROACH TO CARBOCYCLES AND HETEROCYCLES [J]. TETRAHEDRON, 1986, 42 (11) : 2831 - 2846

[10] STEREOSPECIFIC DIENE SYNTHESIS USING ACETYLENE CARBOCUPRATION - PREPARATION OF NAVEL ORANGEWORM PHEROMONE AND LEUKOTRIENE ANALOGS [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1986, (10): : 1809 - 1816