A convergent synthesis of (+)-parviflorin, (+)-squamocin K, and (+)-5S-hydroxyparviflorin

[1] SELECTIVE ASYMMETRIC DIHYDROXYLATION OF POLYENES [J]. TETRAHEDRON, 1995, 51 (05) : 1345 - 1376

[2] CAVE A, 1993, RECENT ADV PHYTOCHEM, V27, P167

[3] A USEFUL 12-I-5 TRIACETOXYPERIODINANE (THE DESS-MARTIN PERIODINANE) FOR THE SELECTIVE OXIDATION OF PRIMARY OR SECONDARY ALCOHOLS AND A VARIETY OF RELATED 12-I-5 SPECIES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (19) : 7277 - 7287

[4] DEVRIES VG, 1976, J MED CHEM, V19, P946, DOI 10.1021/jm00229a018

[5] SYNTHESES OF ACETOGENINS OF ANNONACEAE - A NEW CLASS OF BIOACTIVE POLYKETIDES [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (09) : 359 - 365

[6] NOVEL REAGENT SYSTEM FOR CONVERTING A HYDROXY-GROUP INTO AN IODO-GROUP IN CARBOHYDRATES WITH INVERSION OF CONFIGURATION .3. [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1982, (03): : 681 - 683

[7] GU ZM, 1993, HETEROCYCLES, V36, P2221

[8] Annonaceous acetogenins - Synthetic approaches towards a novel class of natural products [J]. SYNTHESIS-STUTTGART, 1995, (12): : 1447 - &

[9] TOTAL SYNTHESIS OF THE POTENT ANTITUMOR, BIS-TETRAHYDROFURANYL ANNONACEOUS ACETOGENINS (+)-ASIMICIN AND (+)-BULLATACIN [J]. TETRAHEDRON LETTERS, 1995, 36 (12) : 1981 - 1984

[10] Highly efficient synthesis of the potent antitumor annonaceous acetogenin (+)-parviflorin [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (07) : 1801 - 1802

[1] SELECTIVE ASYMMETRIC DIHYDROXYLATION OF POLYENES [J]. TETRAHEDRON, 1995, 51 (05) : 1345 - 1376

[2] CAVE A, 1993, RECENT ADV PHYTOCHEM, V27, P167

[3] A USEFUL 12-I-5 TRIACETOXYPERIODINANE (THE DESS-MARTIN PERIODINANE) FOR THE SELECTIVE OXIDATION OF PRIMARY OR SECONDARY ALCOHOLS AND A VARIETY OF RELATED 12-I-5 SPECIES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (19) : 7277 - 7287

[4] DEVRIES VG, 1976, J MED CHEM, V19, P946, DOI 10.1021/jm00229a018

[5] SYNTHESES OF ACETOGENINS OF ANNONACEAE - A NEW CLASS OF BIOACTIVE POLYKETIDES [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (09) : 359 - 365

[6] NOVEL REAGENT SYSTEM FOR CONVERTING A HYDROXY-GROUP INTO AN IODO-GROUP IN CARBOHYDRATES WITH INVERSION OF CONFIGURATION .3. [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1982, (03): : 681 - 683

[7] GU ZM, 1993, HETEROCYCLES, V36, P2221

[8] Annonaceous acetogenins - Synthetic approaches towards a novel class of natural products [J]. SYNTHESIS-STUTTGART, 1995, (12): : 1447 - &

[9] TOTAL SYNTHESIS OF THE POTENT ANTITUMOR, BIS-TETRAHYDROFURANYL ANNONACEOUS ACETOGENINS (+)-ASIMICIN AND (+)-BULLATACIN [J]. TETRAHEDRON LETTERS, 1995, 36 (12) : 1981 - 1984

[10] Highly efficient synthesis of the potent antitumor annonaceous acetogenin (+)-parviflorin [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (07) : 1801 - 1802