TOTAL SYNTHESIS OF (+/-)-ISOAVENACIOLIDE AND (+/-)-AVENACIOLIDE

[1] 2 NEW MOULD METABOLITES RELATED TO AVENACIOLIDE [J]. JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1971, (13): : 2431 - &

[2] SYNTHESIS OF BIS-GAMMA-LACTONES FROM DIACETONE GLUCOSE .4. OPTICALLY-ACTIVE AVENACIOLIDE AND ISOAVENACIOLIDE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (24) : 4781 - 4786

[3] SYNTHESIS OF OPTICALLY-ACTIVE AVENACIOLIDE FROM D-GLUCOSE - CORRECT STEREOCHEMISTRY OF NATURAL PRODUCT [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (13) : 3870 - 3871

[4] ANDERSON RC, 1977, TETRAHEDRON LETT, P2865

[5] PREFERENCE FOR 6-EXO-TRIGONAL CLOSURES OF "OMEGA-HYDROXY-ALPHABETA-UNSATURATED ESTERS [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (03) : 77 - 77

[6] 5-ENDO-TRIGONAL REACTIONS - DISFAVORED RING-CLOSURE [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 736 - 738

[7] APPROACH VECTOR ANALYSIS - STEREOCHEMICAL APPROACH TO REACTIVITY [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 738 - 741

[8] RULES FOR RING-CLOSURE - RING FORMATION BY CONJUGATE ADDITION OF OXYGEN NUCLEOPHILES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1977, 42 (24) : 3846 - 3852

[9] RULES FOR RING-CLOSURE [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 734 - 736

[10] RULES FOR RING-CLOSURE - STEREOELECTRONIC CONTROL IN ENDOCYCLIC ALKYLATION OF KETONE ENOLATES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (07) : 233 - 235

[1] 2 NEW MOULD METABOLITES RELATED TO AVENACIOLIDE [J]. JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1971, (13): : 2431 - &

[2] SYNTHESIS OF BIS-GAMMA-LACTONES FROM DIACETONE GLUCOSE .4. OPTICALLY-ACTIVE AVENACIOLIDE AND ISOAVENACIOLIDE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (24) : 4781 - 4786

[3] SYNTHESIS OF OPTICALLY-ACTIVE AVENACIOLIDE FROM D-GLUCOSE - CORRECT STEREOCHEMISTRY OF NATURAL PRODUCT [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (13) : 3870 - 3871

[4] ANDERSON RC, 1977, TETRAHEDRON LETT, P2865

[5] PREFERENCE FOR 6-EXO-TRIGONAL CLOSURES OF "OMEGA-HYDROXY-ALPHABETA-UNSATURATED ESTERS [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (03) : 77 - 77

[6] 5-ENDO-TRIGONAL REACTIONS - DISFAVORED RING-CLOSURE [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 736 - 738

[7] APPROACH VECTOR ANALYSIS - STEREOCHEMICAL APPROACH TO REACTIVITY [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 738 - 741

[8] RULES FOR RING-CLOSURE - RING FORMATION BY CONJUGATE ADDITION OF OXYGEN NUCLEOPHILES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1977, 42 (24) : 3846 - 3852

[9] RULES FOR RING-CLOSURE [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 734 - 736

[10] RULES FOR RING-CLOSURE - STEREOELECTRONIC CONTROL IN ENDOCYCLIC ALKYLATION OF KETONE ENOLATES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1977, (07) : 233 - 235