167 related articles for article (PubMed ID: 19402635)
1. Water overcomes methyl group directing effects in epoxide-opening cascades.
Morten CJ; Jamison TF
J Am Chem Soc; 2009 May; 131(19):6678-9. PubMed ID: 19402635
[TBL] [Abstract][Full Text] [Related]
2. Epoxide-opening cascades promoted by water.
Vilotijevic I; Jamison TF
Science; 2007 Aug; 317(5842):1189-92. PubMed ID: 17761875
[TBL] [Abstract][Full Text] [Related]
3. Ladder polyether synthesis via epoxide-opening cascades using a disappearing directing group.
Simpson GL; Heffron TP; Merino E; Jamison TF
J Am Chem Soc; 2006 Feb; 128(4):1056-7. PubMed ID: 16433504
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of the ABC framework of tamulamides A and B.
Kelley EH; Jamison TF
Bioorg Med Chem; 2018 Oct; 26(19):5327-5335. PubMed ID: 29729986
[TBL] [Abstract][Full Text] [Related]
5. Synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascades.
Vilotijevic I; Jamison TF
Mar Drugs; 2010 Mar; 8(3):763-809. PubMed ID: 20411125
[TBL] [Abstract][Full Text] [Related]
6. The development of endo-selective epoxide-opening cascades in water.
Morten CJ; Byers JA; Van Dyke AR; Vilotijevic I; Jamison TF
Chem Soc Rev; 2009 Nov; 38(11):3175-92. PubMed ID: 19847350
[TBL] [Abstract][Full Text] [Related]
7. Tetrahydropyran formation by rearrangement of an epoxy ester: a model for the biosynthesis of marine polyether toxins.
Giner JL
J Org Chem; 2005 Jan; 70(2):721-4. PubMed ID: 15651829
[TBL] [Abstract][Full Text] [Related]
8. Organic chemistry: zippier synthesis in water.
Inoue M
Nature; 2007 Oct; 449(7163):667-9. PubMed ID: 17928848
[No Abstract] [Full Text] [Related]
9. Evidence that epoxide-opening cascades promoted by water are stepwise and become faster and more selective after the first cyclization.
Morten CJ; Byers JA; Jamison TF
J Am Chem Soc; 2011 Feb; 133(6):1902-8. PubMed ID: 21235230
[TBL] [Abstract][Full Text] [Related]
10. Rhodium-catalyzed endo-selective epoxide-opening cascades: formal synthesis of (-)-brevisin.
Armbrust KW; Beaver MG; Jamison TF
J Am Chem Soc; 2015 Jun; 137(21):6941-6. PubMed ID: 25984951
[TBL] [Abstract][Full Text] [Related]
11. [Reaction Development Utilizing the Features of Chemical Elements and Synthesis of Marine Natural Products].
Saito T
Yakugaku Zasshi; 2018; 138(11):1335-1344. PubMed ID: 30381641
[TBL] [Abstract][Full Text] [Related]
12. A dioxane template for highly selective epoxy alcohol cyclizations.
Mousseau JJ; Morten CJ; Jamison TF
Chemistry; 2013 Jul; 19(30):10004-16. PubMed ID: 23775936
[TBL] [Abstract][Full Text] [Related]
13. Studies on the Biomimetic Synthesis of Marine Ladder Polyethers via Endo-Selective Epoxide-to-Epoxonium Ring-Opening Cascades.
Xiao JX; Li FX; Ren SJ; Qu J
Angew Chem Int Ed Engl; 2024 May; ():e202403597. PubMed ID: 38752455
[TBL] [Abstract][Full Text] [Related]
14. Epoxide-opening cascades in the synthesis of polycyclic polyether natural products.
Vilotijevic I; Jamison TF
Angew Chem Int Ed Engl; 2009; 48(29):5250-81. PubMed ID: 19572302
[TBL] [Abstract][Full Text] [Related]
15. Ladder polyether synthesis via epoxide-opening cascades directed by a disappearing trimethylsilyl group.
Heffron TP; Simpson GL; Merino E; Jamison TF
J Org Chem; 2010 Apr; 75(8):2681-701. PubMed ID: 20302314
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of the WXYZA' domain of maitotoxin.
Nicolaou KC; Baker TM; Nakamura T
J Am Chem Soc; 2011 Jan; 133(2):220-6. PubMed ID: 21166430
[TBL] [Abstract][Full Text] [Related]
17. An Endo-Selective Epoxide-Opening Cascade for the Fast Assembly of the Polycyclic Core Structure of Marine Ladder Polyethers.
Li FX; Ren SJ; Li PF; Yang P; Qu J
Angew Chem Int Ed Engl; 2020 Oct; 59(42):18473-18478. PubMed ID: 32666578
[TBL] [Abstract][Full Text] [Related]
18. Synthetic studies on maitotoxin. 2. Stereoselective synthesis of the WXYZA'-ring system.
Morita M; Haketa T; Koshino H; Nakata T
Org Lett; 2008 May; 10(9):1679-82. PubMed ID: 18393507
[TBL] [Abstract][Full Text] [Related]
19. A flexible approach toward trans-fused polycyclic tetrahydropyrans. A synthesis of prymnesin and yessotoxin units.
Trost BM; Rhee YH
Org Lett; 2004 Nov; 6(23):4311-3. PubMed ID: 15524471
[TBL] [Abstract][Full Text] [Related]
20. SmI2-induced cyclizations and their applications in natural product synthesis.
Nakata T
Chem Rec; 2010 Jun; 10(3):159-72. PubMed ID: 20503205
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
