Practical total synthesis of fuligocandins A and B

Synlett

Volumn , Issue 16, 2010, Pages 2498-2502

  Arai, Midori A ^a   Seto, Junya ^a   Ahmed, Firoj ^a   Uchiyama, Kento ^a   Ishibashi, Masami ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

fuligocandin; Meyer Schuster rearrangement; myxomycete; total synthesis; TRAIL

Indexed keywords

CARBON 11; FULIGOCANDIN A; FULIGOCANDIN B; NATURAL PRODUCT; PROLINE DERIVATIVE; SULFUR; UNCLASSIFIED DRUG;

ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ISOMER; MYXOGASTRIA; OPTICAL ROTATION; RACEMIZATION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 77957122602     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1258547     Document Type: Article

References (6)

1. Nakatani S, Yamamoto Y, Hayashi M, Komiyama K, Ishibashi M, Chem. Pharm. Bull. 2004 52 368
2. Hasegawa H, Yamada Y, Komiyama K, Hayashi M, Ishibashi M, Sunazuka T, Izuhara T, Sugahara K, Tsuruda K, Masuda M, Takasu N, Tsukasaki K, Tomonaga M, Kamihira S, Blood 2007 110 1664
3. For a reported synthesis of fuligocandin A, see:, More S S., Shanmughapriya D, Lingam Y, Patel N B., Synth. Commun. 2009 39 2058
4. For the synthesis of racemic fuligocandins A and B, see:, Pettersson B, Hasimbegovic V, Bergman J, Tetrahedron Lett. 2010 51 238
5. For a reported Meyer-Schuster rearrangement of N -Boc lactam, see:, Sun C, Lin X, Weinreb S, J. Org. Chem. 2006 71 3159
6. A Meyer-Schuster rearrangement of N -alkylated succinimide gave E -isomer as a main product:, Mamouni A, Dach A, Decroix B, Synth. Commun. 1998 28 1839