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631 related items for PubMed ID: 15960492
1. 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 24; 70(13):4954-61. PubMed ID: 15960492 [Abstract] [Full Text] [Related]
2. A concise approach to the core structures of pinnaic acid and halichlorine. Yang SH, Clark GR, Caprio V. Org Biomol Chem; 2009 Jul 21; 7(14):2981-90. PubMed ID: 19582309 [Abstract] [Full Text] [Related]
6. Total synthesis of the marine alkaloid halichlorine: development and use of a general route to chiral piperidines. Liu D, Acharya HP, Yu M, Wang J, Yeh VS, Kang S, Chiruta C, Jachak SM, Clive DL. J Org Chem; 2009 Oct 02; 74(19):7417-28. PubMed ID: 19739615 [Abstract] [Full Text] [Related]
9. Asymmetric construction of three contiguous stereogenic centers by conjugate addition-alkylation of lithium ester enolate. Yamamoto Y, Yasuda Y, Nasu H, Tomioka K. Org Lett; 2009 May 07; 11(9):2007-9. PubMed ID: 19354281 [Abstract] [Full Text] [Related]
10. Efficient construction of stereodefined alpha-alkylidene aza-cycloketones via beta-amino-alkenyllithium: straightforward and protection-free synthesis of allopumiliotoxin 267A. Wang B, Zhong Z, Lin GQ. Org Lett; 2009 May 07; 11(9):2011-4. PubMed ID: 19334712 [Abstract] [Full Text] [Related]
11. Total synthesis of (+/-)-halichlorine, (+/-)-pinnaic acid, and (+/-)-tauropinnaic acid. Christie HS, Heathcock CH. Proc Natl Acad Sci U S A; 2004 Aug 17; 101(33):12079-84. PubMed ID: 15299146 [Abstract] [Full Text] [Related]
12. Asymmetric aza-Wittig reactions: enantioselective synthesis of beta-quaternary azacycles. Lertpibulpanya D, Marsden SP, Rodriguez-Garcia I, Kilner CA. Angew Chem Int Ed Engl; 2006 Jul 24; 45(30):5000-2. PubMed ID: 16819749 [No Abstract] [Full Text] [Related]
14. An imine addition/ring-closing metathesis approach to the spirocyclic core of halichlorine and pinnaic acid. Wright DL, Schulte II JP, Page MA. Org Lett; 2000 Jun 29; 2(13):1847-50. PubMed ID: 10891173 [Abstract] [Full Text] [Related]
15. Pinnarine, another member of the halichlorine family. Isolation and preparation from pinnaic acid. Xu S, Yoshimura H, Maru N, Ohno O, Arimoto H, Uemura D. J Nat Prod; 2011 May 27; 74(5):1323-6. PubMed ID: 21410164 [Abstract] [Full Text] [Related]
16. Total synthesis of (-)-reveromycin a. El Sous M, Ganame D, Tregloan PA, Rizzacasa MA. Org Lett; 2004 Aug 19; 6(17):3001-4. PubMed ID: 15330668 [Abstract] [Full Text] [Related]
17. Synthesis of spirodienones by intramolecular ipso-cyclization of N-methoxy-(4-halogenophenyl)amides using [hydroxy(tosyloxy)iodo]benzene in trifluoroethanol. Miyazawa E, Sakamoto T, Kikugawa Y. J Org Chem; 2003 Jun 27; 68(13):5429-32. PubMed ID: 12816516 [Abstract] [Full Text] [Related]
18. Convergent approach to complex spirocyclic pyrans: practical synthesis of the oxa-pinnaic acid core. Ferrari FD, Pasqua AE, Ledgard AJ, Marquez R. Org Biomol Chem; 2013 Jun 07; 11(21):3469-76. PubMed ID: 23589153 [Abstract] [Full Text] [Related]
19. Synthetic studies toward halichlorine: complex azaspirocycle formation with use of an NBS-promoted semipinacol reaction. Hurley PB, Dake GR. J Org Chem; 2008 Jun 06; 73(11):4131-8. PubMed ID: 18444680 [Abstract] [Full Text] [Related]