253 related articles for article (PubMed ID: 15976860)
1. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation.
Paterson I; Chen DY; Coster MJ; Aceña JL; Bach J; Wallace DJ
Org Biomol Chem; 2005 Jul; 3(13):2431-40. PubMed ID: 15976860
[TBL] [Abstract][Full Text] [Related]
2. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment.
Paterson I; Coster MJ; Chen DY; Aceña JL; Bach J; Keown LE; Trieselmann T
Org Biomol Chem; 2005 Jul; 3(13):2420-30. PubMed ID: 15976859
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncation.
Paterson I; Aceña JL; Bach J; Chen DY; Coster MJ
Chem Commun (Camb); 2003 Feb; (4):462-3. PubMed ID: 12638950
[TBL] [Abstract][Full Text] [Related]
4. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the AB-spiroacetal segment.
Paterson I; Coster MJ; Chen DY; Oballa RM; Wallace DJ; Norcross RD
Org Biomol Chem; 2005 Jul; 3(13):2399-409. PubMed ID: 15976857
[TBL] [Abstract][Full Text] [Related]
5. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment.
Paterson I; Coster MJ; Chen DY; Gibson KR; Wallace DJ
Org Biomol Chem; 2005 Jul; 3(13):2410-9. PubMed ID: 15976858
[TBL] [Abstract][Full Text] [Related]
6. Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2).
Heathcock CH; McLaughlin M; Medina J; Hubbs JL; Wallace GA; Scott R; Claffey MM; Hayes CJ; Ott GR
J Am Chem Soc; 2003 Oct; 125(42):12844-9. PubMed ID: 14558833
[TBL] [Abstract][Full Text] [Related]
7. Towards the combinatorial synthesis of spongistatin fragment libraries by using asymmetric aldol reactions on solid support.
Paterson I; Gottschling D; Menche D
Chem Commun (Camb); 2005 Jul; (28):3568-70. PubMed ID: 16010326
[TBL] [Abstract][Full Text] [Related]
8. A modular approach to marine macrolide construction. 4. Assembly of C36-C51 and C29-C44 building blocks and evaluation of key coupling reactions targeting spongistatin 1 (altohyrtin A).
Ciblat S; Kim J; Stewart CA; Wang J; Forgione P; Clyne D; Paquette LA
Org Lett; 2007 Feb; 9(4):719-22. PubMed ID: 17286379
[TBL] [Abstract][Full Text] [Related]
9. Synthesis and biological evaluation of 10,11-dihydrodictyostatin, a potent analogue of the marine anticancer agent dictyostatin.
Paterson I; Gardner NM; Poullennec KG; Wright AE
J Nat Prod; 2008 Mar; 71(3):364-9. PubMed ID: 18081257
[TBL] [Abstract][Full Text] [Related]
10. Total synthesis and biological evaluation of (+)-neopeltolide and its analogues.
Fuwa H; Saito A; Naito S; Konoki K; Yotsu-Yamashita M; Sasaki M
Chemistry; 2009 Nov; 15(46):12807-18. PubMed ID: 19882704
[TBL] [Abstract][Full Text] [Related]
11. Total synthesis and biological evaluation of potent analogues of dictyostatin: modification of the C2-C6 dienoate region.
Paterson I; Gardner NM; Guzmán E; Wright AE
Bioorg Med Chem Lett; 2008 Dec; 18(23):6268-72. PubMed ID: 18951787
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of the ABC tricyclic fragment of the pectenotoxins via stereocontrolled cyclization of a gamma-hydroxyepoxide appended to the AB spiroacetal unit.
Halim R; Brimble MA; Merten J
Org Biomol Chem; 2006 Apr; 4(7):1387-99. PubMed ID: 16557329
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of the ABC fragment of the pectenotoxins.
Halim R; Brimble MA; Merten J
Org Lett; 2005 Jun; 7(13):2659-62. PubMed ID: 15957915
[TBL] [Abstract][Full Text] [Related]
14. Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration.
Smith AB; Zhu W; Shirakami S; Sfouggatakis C; Doughty VA; Bennett CS; Sakamoto Y
Org Lett; 2003 Mar; 5(5):761-4. PubMed ID: 12605509
[TBL] [Abstract][Full Text] [Related]
15. A second-generation synthesis of the C1-C28 portion of the altohyrtins (spongistatins).
Hubbs JL; Heathcock CH
J Am Chem Soc; 2003 Oct; 125(42):12836-43. PubMed ID: 14558832
[TBL] [Abstract][Full Text] [Related]
16. The stereocontrolled total synthesis of spirastrellolide A methyl ester. Fragment coupling studies and completion of the synthesis.
Paterson I; Anderson EA; Dalby SM; Lim JH; Maltas P
Org Biomol Chem; 2012 Aug; 10(30):5873-86. PubMed ID: 22504907
[TBL] [Abstract][Full Text] [Related]
17. The laulimalide family: total synthesis and biological evaluation of neolaulimalide, isolaulimalide, laulimalide and a nonnatural analogue.
Gollner A; Altmann KH; Gertsch J; Mulzer J
Chemistry; 2009 Jun; 15(24):5979-97. PubMed ID: 19402092
[TBL] [Abstract][Full Text] [Related]
18. Short diastereoselective synthesis of the C1-C13 (AB spiroacetal) and C17-C28 fragments (CD spiroacetal) of spongistatin 1 and 2 through double chain-elongation reactions.
Flowers CL; Vogel P
Chemistry; 2010 Dec; 16(47):14074-82. PubMed ID: 20963739
[TBL] [Abstract][Full Text] [Related]
19. Stereoselective synthesis of premisakinolide A, the monomeric counterpart of the marine 40-membered dimeric macrolide misakinolide A.
Nakamura R; Tanino K; Miyashita M
Org Lett; 2005 Jul; 7(14):2929-32. PubMed ID: 15987172
[TBL] [Abstract][Full Text] [Related]
20. Total synthesis of apoptolidin: completion of the synthesis and analogue synthesis and evaluation.
Nicolaou KC; Li Y; Sugita K; Monenschein H; Guntupalli P; Mitchell HJ; Fylaktakidou KC; Vourloumis D; Giannakakou P; O'Brate A
J Am Chem Soc; 2003 Dec; 125(50):15443-54. PubMed ID: 14664590
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
