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.
185 related articles for article (PubMed ID: 16235944)
1. Progress in the synthesis of the lituarines: stereocontrol in sequential C-C bond formation on a spirobutenolide template. Robertson J; Dallimore JW Org Lett; 2005 Oct; 7(22):5007-10. PubMed ID: 16235944 [TBL] [Abstract][Full Text] [Related]
2. Syntheses of the C(1-6) and C(19-24) fragments of lituarines A, B, and C. Robertson J; Dallimore JW; Meo P Org Lett; 2004 Oct; 6(21):3857-9. PubMed ID: 15469367 [TBL] [Abstract][Full Text] [Related]
3. Stereoselective synthesis of the lituarine tricyclic spiroacetal. Robertson J; Meo P; Dallimore JW; Doyle BM; Hoarau C Org Lett; 2004 Oct; 6(21):3861-3. PubMed ID: 15469368 [TBL] [Abstract][Full Text] [Related]
4. First total synthesis of (-)-AL-2. Miyakoshi N; Mukai C Org Lett; 2003 Jun; 5(13):2335-8. PubMed ID: 12816442 [TBL] [Abstract][Full Text] [Related]
5. Lituarine synthetic studies. An efficient, stereocontrolled construction of the common c(7-19) tricyclic spiroketal fragment. Smith AB; Frohn M Org Lett; 2001 Nov; 3(24):3979-82. PubMed ID: 11720584 [TBL] [Abstract][Full Text] [Related]
6. Total syntheses of the assigned structures of lituarines B and C. Smith AB; Duffey MO; Basu K; Walsh SP; Suennemann HW; Frohn M J Am Chem Soc; 2008 Jan; 130(2):422-3. PubMed ID: 18095694 [No Abstract] [Full Text] [Related]
7. Total syntheses of naturally occurring diacetylenic spiroacetal enol ethers. Miyakoshi N; Aburano D; Mukai C J Org Chem; 2005 Jul; 70(15):6045-52. PubMed ID: 16018702 [TBL] [Abstract][Full Text] [Related]
8. Development of the intramolecular Prins cyclization/Schmidt reaction for the construction of the azaspiro[4,4]nonane: application to the formal synthesis of (±)-stemonamine. Chen ZH; Tu YQ; Zhang SY; Zhang FM Org Lett; 2011 Feb; 13(4):724-7. PubMed ID: 21229997 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. N-heterocyclic carbene catalyzed reaction of enals and 1,2-dicarbonyl compounds: stereoselective synthesis of spiro gamma-butyrolactones. Nair V; Vellalath S; Poonoth M; Mohan R; Suresh E Org Lett; 2006 Feb; 8(3):507-9. PubMed ID: 16435871 [TBL] [Abstract][Full Text] [Related]
11. Formal synthesis of berkelic acid: a lesson in α-alkylation chemistry. McLeod MC; Wilson ZE; Brimble MA J Org Chem; 2012 Jan; 77(1):400-16. PubMed ID: 22077770 [TBL] [Abstract][Full Text] [Related]
12. Stereocontrol of 5,5-spiroketals in the synthesis of cephalosporolide H epimers. Tlais SF; Dudley GB Org Lett; 2010 Oct; 12(20):4698-701. PubMed ID: 20860404 [TBL] [Abstract][Full Text] [Related]
13. An enantioselective formal synthesis of berkelic acid. McLeod MC; Wilson ZE; Brimble MA Org Lett; 2011 Oct; 13(19):5382-5. PubMed ID: 21916400 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Convergent assembly of the spiroacetal subunit of didemnaketal B. Fuwa H; Noji S; Sasaki M Org Lett; 2010 Nov; 12(22):5354-7. PubMed ID: 21028885 [TBL] [Abstract][Full Text] [Related]
16. Synthesis of the core structure of acutumine. Reeder MD; Srikanth GS; Jones SB; Castle SL Org Lett; 2005 Mar; 7(6):1089-92. PubMed ID: 15760146 [TBL] [Abstract][Full Text] [Related]
17. An efficient and enantioselective approach to the azaspirocyclic core of alkaloids: formal synthesis of halichlorine and pinnaic acid. Zhang HL; Zhao G; Ding Y; Wu B J Org Chem; 2005 Jun; 70(13):4954-61. PubMed ID: 15960492 [TBL] [Abstract][Full Text] [Related]
18. Diversity-oriented synthesis of polyketide natural products via iterative chemo- and stereoselective functionalization of polyenoates: development of a unified approach for the C(1-19) segments of lituarines A-C. Smith AB; Walsh SP; Frohn M; Duffey MO Org Lett; 2005 Jan; 7(1):139-42. PubMed ID: 15624997 [TBL] [Abstract][Full Text] [Related]
19. Lambertellols A and B, novel 3,4-dihydronaphthalen-1(2H)-ones with spiro-butenolide produced by Lambertella sp.1346. Murakami T; Morikawa Y; Hashimoto M; Okuno T; Harada Y Org Lett; 2004 Jan; 6(2):157-60. PubMed ID: 14723517 [TBL] [Abstract][Full Text] [Related]
20. Structural revision of cephalosporolide J and bassianolone. Song L; Lee KH; Lin Z; Tong R J Org Chem; 2014 Feb; 79(3):1493-7. PubMed ID: 24417265 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]