These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
182 related articles for article (PubMed ID: 11304197)
1. Total synthesis of rutamycin B and oligomycin C. Panek JS; Jain NF J Org Chem; 2001 Apr; 66(8):2747-56. PubMed ID: 11304197 [TBL] [Abstract][Full Text] [Related]
2. Total synthesis of rutamycin B, a macrolide antibiotic from Streptomyces aureofaciens. White JD; Hanselmann R; Jackson RW; Porter WJ; Ohba Y; Tiller T; Wang S J Org Chem; 2001 Jul; 66(15):5217-31. PubMed ID: 11463276 [TBL] [Abstract][Full Text] [Related]
3. Asymmetric crotylation reactions in synthesis of polypropionate-derived macrolides: application to total synthesis of oleandolide. Hu T; Takenaka N; Panek JS J Am Chem Soc; 2002 Oct; 124(43):12806-15. PubMed ID: 12392427 [TBL] [Abstract][Full Text] [Related]
4. Asymmetric total synthesis of spongistatins 1 and 2. Crimmins MT; Katz JD; Washburn DG; Allwein SP; McAtee LF J Am Chem Soc; 2002 May; 124(20):5661-3. PubMed ID: 12010038 [TBL] [Abstract][Full Text] [Related]
5. Crotylsilane reagents in the synthesis of complex polyketide natural products: total synthesis of (+)-discodermolide. Arefolov A; Panek JS J Am Chem Soc; 2005 Apr; 127(15):5596-603. PubMed ID: 15826198 [TBL] [Abstract][Full Text] [Related]
6. Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 5. Stereoselective synthesis of the C13-C23 part via condensation of two fragments, C13-C17 and C18-C21, by taking advantage of the 3,4-dimethoxybenzyl protecting group. Zheng BZ; Maeda H; Mori M; Kusaka S; Yonemitsu O; Matsushima T; Nakajima N; Uenishi J Chem Pharm Bull (Tokyo); 1999 Sep; 47(9):1288-96. PubMed ID: 10517009 [TBL] [Abstract][Full Text] [Related]
7. Total synthesis of cruentaren B. Chakraborty TK; Chattopadhyay AK J Org Chem; 2008 May; 73(9):3578-81. PubMed ID: 18363370 [TBL] [Abstract][Full Text] [Related]
8. [Total synthesis of antitumor macrolide, rhizoxin and chemistry of acylsilane]. Nakada M Yakugaku Zasshi; 1997 Aug; 117(8):486-508. PubMed ID: 9306725 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. The first total synthesis of concanamycin f (concanolide a). Toshima K; Jyojima T; Miyamoto N; Katohno M; Nakata M; Matsumura S J Org Chem; 2001 Mar; 66(5):1708-15. PubMed ID: 11262117 [TBL] [Abstract][Full Text] [Related]
12. Enantioselective total synthesis of (+)-amphidinolide t1. Ghosh AK; Liu C J Am Chem Soc; 2003 Mar; 125(9):2374-5. PubMed ID: 12603108 [TBL] [Abstract][Full Text] [Related]
13. Synthesis of C13-C25 fragment of 24-demethylbafilomycin C(1) via diastereoselective aldol reactions of a ketone boron enolate as the key step. Guan Y; Wu J; Sun L; Dai WM J Org Chem; 2007 Jun; 72(13):4953-60. PubMed ID: 17518500 [TBL] [Abstract][Full Text] [Related]
15. Synthesis of two subunits of the macrolide domain of the immunosuppressive agent sanglifehrin a and assembly of a macrolactone precursor. application of masamune anti-aldol condensation. Suttisintong K; White JD J Org Chem; 2015 Feb; 80(4):2249-62. PubMed ID: 25584782 [TBL] [Abstract][Full Text] [Related]
16. Synthesis of the C1-C28 Portion of Spongistatin 1 (Altohyrtin A). Claffey MM; Hayes CJ; Heathcock CH J Org Chem; 1999 Oct; 64(22):8267-8274. PubMed ID: 11674747 [TBL] [Abstract][Full Text] [Related]
17. Total synthesis of the epidermal growth factor inhibitor (-)-reveromycin B. Cuzzupe AN; Hutton CA; Lilly MJ; Mann RK; McRae KJ; Zammit SC; Rizzacasa MA J Org Chem; 2001 Apr; 66(7):2382-93. PubMed ID: 11281779 [TBL] [Abstract][Full Text] [Related]
18. A convergent three-component total synthesis of the powerful immunosuppressant (-)-sanglifehrin a. Paquette LA; Duan M; Konetzki I; Kempmann C J Am Chem Soc; 2002 Apr; 124(16):4257-70. PubMed ID: 11960455 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals. Holson EB; Roush WR Org Lett; 2002 Oct; 4(21):3723-5. PubMed ID: 12375928 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]