Stereochemistry of the core structure of the mycolactones

[1] NOVEL STRUCTURE ELUCIDATION OF AAL TOXIN T-A BACKBONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (11) : 4995 - 4996

[2] BOYLE CD, 1995, TETRAHEDRON LETT, V36, P5695, DOI 10.1016/00404-0399(50)11263-

[3] CHIRAL SYNTHESIS VIA ORGANOBORANES .7. DIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF ERYTHRO-BETA-METHYLOMOALLYL AND THREO-BETA-METHYLHOMOALLYL ALCHOLS VIA ENANTIOMERIC (Z)-CROTYLBORANE AND (E)-CROTYLBORANE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (19) : 5919 - 5923

[4] Efficient and highly selective oxidation of primary alcohols to aldehydes by N-chlorosuccinimide mediated by oxoammonium salts [J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (21) : 7452 - 7454

[5] Mycolactone:: A polyketide toxin from Mycobacterium ulcerans required for virulence [J]. SCIENCE, 1999, 283 (5403) : 854 - 857

[6] A Mycobacterium ulcerans toxin, mycolactone, causes apoptosis in guinea pig ulcers and tissue culture cells [J]. INFECTION AND IMMUNITY, 2000, 68 (02) : 877 - 883

[7] CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL-PRODUCTS .32. SYNTHESIS OF ERYTHRONOLIDE A VIA A VERY EFFICIENT MACROLACTONIZATION UNDER USUAL ACYLATION CONDITIONS WITH THE YAMAGUCHI REAGENT [J]. TETRAHEDRON LETTERS, 1990, 31 (44) : 6367 - 6370

[8] RAPID ESTERIFICATION BY MEANS OF MIXED ANHYDRIDE AND ITS APPLICATION TO LARGE-RING LACTONIZATION [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1979, 52 (07) : 1989 - 1993

[9] Toward creation of a universal NMR database for stereochemical assignment: Complete structure of the desertomycin/oasomycin class of natural products [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (09) : 2076 - 2078

[10] Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: The case of two contiguous propionate units [J]. ORGANIC LETTERS, 1999, 1 (13) : 2177 - 2180

[1] NOVEL STRUCTURE ELUCIDATION OF AAL TOXIN T-A BACKBONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (11) : 4995 - 4996

[2] BOYLE CD, 1995, TETRAHEDRON LETT, V36, P5695, DOI 10.1016/00404-0399(50)11263-

[3] CHIRAL SYNTHESIS VIA ORGANOBORANES .7. DIASTEREOSELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF ERYTHRO-BETA-METHYLOMOALLYL AND THREO-BETA-METHYLHOMOALLYL ALCHOLS VIA ENANTIOMERIC (Z)-CROTYLBORANE AND (E)-CROTYLBORANE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (19) : 5919 - 5923

[4] Efficient and highly selective oxidation of primary alcohols to aldehydes by N-chlorosuccinimide mediated by oxoammonium salts [J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (21) : 7452 - 7454

[5] Mycolactone:: A polyketide toxin from Mycobacterium ulcerans required for virulence [J]. SCIENCE, 1999, 283 (5403) : 854 - 857

[6] A Mycobacterium ulcerans toxin, mycolactone, causes apoptosis in guinea pig ulcers and tissue culture cells [J]. INFECTION AND IMMUNITY, 2000, 68 (02) : 877 - 883

[7] CHIRAL SYNTHESIS OF POLYKETIDE-DERIVED NATURAL-PRODUCTS .32. SYNTHESIS OF ERYTHRONOLIDE A VIA A VERY EFFICIENT MACROLACTONIZATION UNDER USUAL ACYLATION CONDITIONS WITH THE YAMAGUCHI REAGENT [J]. TETRAHEDRON LETTERS, 1990, 31 (44) : 6367 - 6370

[8] RAPID ESTERIFICATION BY MEANS OF MIXED ANHYDRIDE AND ITS APPLICATION TO LARGE-RING LACTONIZATION [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1979, 52 (07) : 1989 - 1993

[9] Toward creation of a universal NMR database for stereochemical assignment: Complete structure of the desertomycin/oasomycin class of natural products [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (09) : 2076 - 2078

[10] Toward creation of a universal NMR database for the stereochemical assignment of acyclic compounds: The case of two contiguous propionate units [J]. ORGANIC LETTERS, 1999, 1 (13) : 2177 - 2180