324 related articles for article (PubMed ID: 17608487)
1. Application of ring-closing metathesis for the synthesis of macrocyclic peptidomimetics as inhibitors of HCV NS3 protease.
Velázquez F; Venkatraman S; Wu W; Blackman M; Prongay A; Girijavallabhan V; Shih NY; Njoroge FG
Org Lett; 2007 Aug; 9(16):3061-4. PubMed ID: 17608487
[TBL] [Abstract][Full Text] [Related]
2. Efficient large-scale synthesis of BILN 2061, a potent HCV protease inhibitor, by a convergent approach based on ring-closing metathesis.
Yee NK; Farina V; Houpis IN; Haddad N; Frutos RP; Gallou F; Wang XJ; Wei X; Simpson RD; Feng X; Fuchs V; Xu Y; Tan J; Zhang L; Xu J; Smith-Keenan LL; Vitous J; Ridges MD; Spinelli EM; Johnson M; Donsbach K; Nicola T; Brenner M; Winter E; Kreye P; Samstag W
J Org Chem; 2006 Sep; 71(19):7133-45. PubMed ID: 16958506
[TBL] [Abstract][Full Text] [Related]
3. Novel potent macrocyclic inhibitors of the hepatitis C virus NS3 protease: use of cyclopentane and cyclopentene P2-motifs.
Bäck M; Johansson PO; Wångsell F; Thorstensson F; Kvarnström I; Ayesa S; Wähling H; Pelcman M; Jansson K; Lindström S; Wallberg H; Classon B; Rydergård C; Vrang L; Hamelink E; Hallberg A; Rosenquist S; Samuelsson B
Bioorg Med Chem; 2007 Nov; 15(22):7184-202. PubMed ID: 17845856
[TBL] [Abstract][Full Text] [Related]
4. Design, synthesis, and biological activity of m-tyrosine-based 16- and 17-membered macrocyclic inhibitors of hepatitis C virus NS3 serine protease.
Chen KX; Njoroge FG; Pichardo J; Prongay A; Butkiewicz N; Yao N; Madison V; Girijavallabhan V
J Med Chem; 2005 Oct; 48(20):6229-35. PubMed ID: 16190750
[TBL] [Abstract][Full Text] [Related]
5. A convergent synthesis of the macrocyclic core of cytotrienins: application of RCM for macrocyclization.
Evano G; Schaus JV; Panek JS
Org Lett; 2004 Feb; 6(4):525-8. PubMed ID: 14961614
[TBL] [Abstract][Full Text] [Related]
6. Synthesis of diverse macrocyclic peptidomimetics utilizing ring-closing metathesis and solid-phase synthesis.
Barrett AG; Hennessy AJ; Le Vézouët R; Procopiou PA; Seale PW; Stefaniak S; Upton RJ; White AJ; Williams DJ
J Org Chem; 2004 Feb; 69(4):1028-37. PubMed ID: 14961650
[TBL] [Abstract][Full Text] [Related]
7. Versatile approach for the synthesis of novel seven-membered iminocyclitols via ring-closing metathesis dihydroxylation reaction.
Lin CC; Pan YS; Patkar LN; Lin HM; Tzou DL; Subramanian T; Lin CC
Bioorg Med Chem; 2004 Jun; 12(12):3259-67. PubMed ID: 15158794
[TBL] [Abstract][Full Text] [Related]
8. RCM macrocyclization made practical: an efficient synthesis of HCV protease inhibitor BILN 2061.
Shu C; Zeng X; Hao MH; Wei X; Yee NK; Busacca CA; Han Z; Farina V; Senanayake CH
Org Lett; 2008 Mar; 10(6):1303-6. PubMed ID: 18293994
[TBL] [Abstract][Full Text] [Related]
9. Development of a concise and diversity-oriented approach for the synthesis of plecomacrolides via the diene-ene RCM.
Lu K; Huang M; Xiang Z; Liu Y; Chen J; Yang Z
Org Lett; 2006 Mar; 8(6):1193-6. PubMed ID: 16524301
[TBL] [Abstract][Full Text] [Related]
10. Ring-closing metathesis as a basis for the construction of aromatic compounds.
Donohoe TJ; Orr AJ; Bingham M
Angew Chem Int Ed Engl; 2006 Apr; 45(17):2664-70. PubMed ID: 16548035
[TBL] [Abstract][Full Text] [Related]
11. Efficient pyrrole synthesis using double nucleophilic addition to alpha,beta-unsaturated imines with plural nucleophiles.
Shimizu M; Takahashi A; Kawai S
Org Lett; 2006 Aug; 8(16):3585-7. PubMed ID: 16869666
[TBL] [Abstract][Full Text] [Related]
12. A highly convergent and efficient synthesis of a macrocyclic hepatitis C virus protease inhibitor BI 201302.
Wei X; Shu C; Haddad N; Zeng X; Patel ND; Tan Z; Liu J; Lee H; Shen S; Campbell S; Varsolona RJ; Busacca CA; Hossain A; Yee NK; Senanayake CH
Org Lett; 2013 Mar; 15(5):1016-9. PubMed ID: 23406520
[TBL] [Abstract][Full Text] [Related]
13. Efficient generation of highly functionalized fused oxazepine frameworks based on a CAN-catalyzed four-component tetrahydropyridine synthesis/ring-closing metathesis sequence.
Sridharan V; Maiti S; Menéndez JC
J Org Chem; 2009 Dec; 74(24):9365-71. PubMed ID: 19921805
[TBL] [Abstract][Full Text] [Related]
14. Parallel solid-phase synthesis of macrocyclic peptidomimetics using Ru-catalyzed ring-closing metathesis and a new application of cross metathesis.
Beaubien S; Hoveyda HR; Vézina M; Marsault E; Tremblay H; Foucher L; Benakli K
Adv Exp Med Biol; 2009; 611():13-4. PubMed ID: 19400073
[No Abstract] [Full Text] [Related]
15. A short route for the synthesis of "sweet" macrocycles via a click-dimerization-ring-closing metathesis approach.
Dörner S; Westermann B
Chem Commun (Camb); 2005 Jun; (22):2852-4. PubMed ID: 15928780
[TBL] [Abstract][Full Text] [Related]
16. A ring-closing metathesis approach toward formal total synthesis of (+)-diplodialide A.
Anand RV; Baktharaman S; Singh VK
J Org Chem; 2003 Apr; 68(8):3356-9. PubMed ID: 12688821
[TBL] [Abstract][Full Text] [Related]
17. Benzoylureas as removable cis amide inducers: synthesis of cyclic amides via ring closing metathesis (RCM).
Brady RM; Khakham Y; Lessene G; Baell JB
Org Biomol Chem; 2011 Feb; 9(3):656-8. PubMed ID: 21088766
[TBL] [Abstract][Full Text] [Related]
18. Formal synthesis of optically active ingenol via ring-closing olefin metathesis.
Watanabe K; Suzuki Y; Aoki K; Sakakura A; Suenaga K; Kigoshi H
J Org Chem; 2004 Nov; 69(23):7802-8. PubMed ID: 15527254
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic.
Oishi S; Karki RG; Shi ZD; Worthy KM; Bindu L; Chertov O; Esposito D; Frank P; Gillette WK; Maderia M; Hartley J; Nicklaus MC; Barchi JJ; Fisher RJ; Burke TR
Bioorg Med Chem; 2005 Apr; 13(7):2431-8. PubMed ID: 15755645
[TBL] [Abstract][Full Text] [Related]
20. Synthesis of 3-hydroxypyridines using ruthenium-catalyzed ring-closing olefin metathesis.
Yoshida K; Kawagoe F; Hayashi K; Horiuchi S; Imamoto T; Yanagisawa A
Org Lett; 2009 Feb; 11(3):515-8. PubMed ID: 19117401
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]