Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids

[1] Abe F, 1998, CHEM PHARM BULL, V46, P1235

[2] Convergent synthesis of the C31-C46 domain of the phorboxazole natural products [J]. TETRAHEDRON LETTERS, 1998, 39 (3-4) : 183 - 186

[3] KR025, a new cytotoxic compound from Myxococcus fulvus [J]. JOURNAL OF NATURAL PRODUCTS, 1999, 62 (03): : 495 - 496

[4] Convergent synthesis of dolastatin 15 by solid phase coupling of an N-methylamino acid [J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (02) : 405 - 411

[5] Epostatin, new inhibitor of dipeptidyl peptidase II, produced by Streptomyces sp. MJ995-OF5 -: II.: Structure elucidation [J]. JOURNAL OF ANTIBIOTICS, 1998, 51 (03) : 372 - 373

[6] A biomimetic approach to the discorhabdin alkaloids: Total syntheses of discorhabdins C and E and dethiadiscorhabdin D [J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (01) : 16 - 22

[7] Bae MA, 1998, J MICROBIOL BIOTECHN, V8, P455

[8] YUA001, a novel aldose reductase inhibitor isolated from alkalophilic Corynebacterium sp. YUA25 -: I.: Taxonomy, fermentation, isolation and characterization [J]. JOURNAL OF ANTIBIOTICS, 1998, 51 (10) : 902 - 907

[9] Baldwin JE, 1998, ANGEW CHEM INT EDIT, V37, P2661, DOI 10.1002/(SICI)1521-3773(19981016)37:19<2661::AID-ANIE2661>3.0.CO

[10] 2-D

[1] Abe F, 1998, CHEM PHARM BULL, V46, P1235

[2] Convergent synthesis of the C31-C46 domain of the phorboxazole natural products [J]. TETRAHEDRON LETTERS, 1998, 39 (3-4) : 183 - 186

[3] KR025, a new cytotoxic compound from Myxococcus fulvus [J]. JOURNAL OF NATURAL PRODUCTS, 1999, 62 (03): : 495 - 496

[4] Convergent synthesis of dolastatin 15 by solid phase coupling of an N-methylamino acid [J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (02) : 405 - 411

[5] Epostatin, new inhibitor of dipeptidyl peptidase II, produced by Streptomyces sp. MJ995-OF5 -: II.: Structure elucidation [J]. JOURNAL OF ANTIBIOTICS, 1998, 51 (03) : 372 - 373

[6] A biomimetic approach to the discorhabdin alkaloids: Total syntheses of discorhabdins C and E and dethiadiscorhabdin D [J]. JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (01) : 16 - 22

[7] Bae MA, 1998, J MICROBIOL BIOTECHN, V8, P455

[8] YUA001, a novel aldose reductase inhibitor isolated from alkalophilic Corynebacterium sp. YUA25 -: I.: Taxonomy, fermentation, isolation and characterization [J]. JOURNAL OF ANTIBIOTICS, 1998, 51 (10) : 902 - 907

[9] Baldwin JE, 1998, ANGEW CHEM INT EDIT, V37, P2661, DOI 10.1002/(SICI)1521-3773(19981016)37:19<2661::AID-ANIE2661>3.0.CO

[10] 2-D