Steroids from sponges: Recent reports

[81] HIV-INHIBITORY NATURAL-PRODUCTS .11. COMPARATIVE-STUDIES OF SULFATED STEROLS FROM MARINE-INVERTEBRATES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (06) : 793 - 797

[82] NEW DELTA-8-5-ALPHA,6-ALPHA-EPOXYSTEROLS AND DELTA-8(14)-5-ALPHA,6-ALPHA-EPOXYSTEROLS FROM THE MARINE SPONGE SPONGIA-OFFICINALIS [J]. STEROIDS, 1993, 58 (03) : 134 - 140

[83] STRUCTURE ELUCIDATION AND SYNTHESIS OF 3-BETA,6-ALPHA-DIHYDROXY-9-OXO-9,11-SECO-5-ALPHA-CHOLEST-7-EN-11-AL, A NOVEL 9,11-SECOSTEROL FROM THE SPONGE SPONGIA-OFFICINALIS [J]. TETRAHEDRON, 1991, 47 (37) : 7937 - 7950

[84] 2 NEW 9,11-SECOSTEROLS FROM THE MARINE SPONGE SPONGIA-OFFICINALIS - SYNTHESIS OF 9,11-SECO-3-BETA,6-ALPHA,11-TRIHYDROXY-5-ALPHA-CHOLEST-7-EN-9-ONE [J]. STEROIDS, 1992, 57 (07) : 344 - 347

[85] 2 NEW POLYHYDROXYLATED STEROLS FROM THE SPONGE DYSIDEA-FRAGILIS [J]. JOURNAL OF NATURAL PRODUCTS, 1992, 55 (07): : 974 - 978

[86] MINALE L, 1978, TETRAHEDRON LETT, P2609

[87] Mishra PD, 1996, INDIAN J CHEM B, V35, P806

[88] SYNTHESIS OF ANTITUMOR MARINE STEROID ARAGUSTEROLS [J]. TETRAHEDRON LETTERS, 1995, 36 (45) : 8231 - 8234

[89] Synthesis of 5-epiaragusterol A [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1997, 7 (06) : 691 - 692

[90] Aragusterols E-H, new 26,27-cyclosterols from the Okinawan marine sponge of the genus Xestospongia and absolute configurations of xestokerols A and B [J]. TETRAHEDRON, 1997, 53 (15) : 5403 - 5412

[81] HIV-INHIBITORY NATURAL-PRODUCTS .11. COMPARATIVE-STUDIES OF SULFATED STEROLS FROM MARINE-INVERTEBRATES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (06) : 793 - 797

[82] NEW DELTA-8-5-ALPHA,6-ALPHA-EPOXYSTEROLS AND DELTA-8(14)-5-ALPHA,6-ALPHA-EPOXYSTEROLS FROM THE MARINE SPONGE SPONGIA-OFFICINALIS [J]. STEROIDS, 1993, 58 (03) : 134 - 140

[83] STRUCTURE ELUCIDATION AND SYNTHESIS OF 3-BETA,6-ALPHA-DIHYDROXY-9-OXO-9,11-SECO-5-ALPHA-CHOLEST-7-EN-11-AL, A NOVEL 9,11-SECOSTEROL FROM THE SPONGE SPONGIA-OFFICINALIS [J]. TETRAHEDRON, 1991, 47 (37) : 7937 - 7950

[84] 2 NEW 9,11-SECOSTEROLS FROM THE MARINE SPONGE SPONGIA-OFFICINALIS - SYNTHESIS OF 9,11-SECO-3-BETA,6-ALPHA,11-TRIHYDROXY-5-ALPHA-CHOLEST-7-EN-9-ONE [J]. STEROIDS, 1992, 57 (07) : 344 - 347

[85] 2 NEW POLYHYDROXYLATED STEROLS FROM THE SPONGE DYSIDEA-FRAGILIS [J]. JOURNAL OF NATURAL PRODUCTS, 1992, 55 (07): : 974 - 978

[86] MINALE L, 1978, TETRAHEDRON LETT, P2609

[87] Mishra PD, 1996, INDIAN J CHEM B, V35, P806

[88] SYNTHESIS OF ANTITUMOR MARINE STEROID ARAGUSTEROLS [J]. TETRAHEDRON LETTERS, 1995, 36 (45) : 8231 - 8234

[89] Synthesis of 5-epiaragusterol A [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1997, 7 (06) : 691 - 692

[90] Aragusterols E-H, new 26,27-cyclosterols from the Okinawan marine sponge of the genus Xestospongia and absolute configurations of xestokerols A and B [J]. TETRAHEDRON, 1997, 53 (15) : 5403 - 5412