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Items: 1 to 20 of 103

1.

Cobalt-mediated synthesis of the tricyclo[5.2.1.0(1,6)]decene framework in solanoeclepin A.

Tsao KW, Cheng CY, Isobe M.

Org Lett. 2012 Oct 19;14(20):5274-7. doi: 10.1021/ol302432d.

PMID:
23020121
2.

Novel synthesis of right segment of solanoeclepin A.

Chuang HY, Isobe M.

Org Lett. 2014 Aug 15;16(16):4166-9. doi: 10.1021/ol501858w.

PMID:
25058474
3.

Novel synthesis of the ABC rings of solanoeclepin A.

Lin YT, Lin FY, Isobe M.

Org Lett. 2014 Nov 21;16(22):5948-51. doi: 10.1021/ol5029755.

PMID:
25376022
4.

Synthesis of the cyclobutanone core of solanoeclepin A intramolecular allene butenolide photocycloaddition.

Hue BT, Dijkink J, Kuiper S, Larson KK, Guziec FS Jr, Goubitz K, Fraanje J, Schenk H, van Maarseveen JH, Hiemstra H.

Org Biomol Chem. 2003 Dec 21;1(24):4364-6.

PMID:
14685306
5.

Formal Synthesis of Solanoeclepin A: Enantioselective Allene Diboration and Intramolecular [2+2] Photocycloaddition for the Construction of the Tricyclic Core.

Kleinnijenhuis RA, Timmer BJ, Lutteke G, Smits JM, de Gelder R, van Maarseveen JH, Hiemstra H.

Chemistry. 2016 Jan 22;22(4):1266-9. doi: 10.1002/chem.201504894.

PMID:
26646583
6.

Total synthesis of solanoeclepin A.

Tanino K, Takahashi M, Tomata Y, Tokura H, Uehara T, Narabu T, Miyashita M.

Nat Chem. 2011 Jun;3(6):484-8. doi: 10.1038/nchem.1044.

PMID:
21602865
7.

Intramolecular photochemical dioxenone-alkene [2 + 2] cycloadditions as an approach to the bicyclo[2.1.1]hexane moiety of solanoeclepin A.

Blaauw RH, Brière JF, de Jong R, Benningshof JC, van Ginkel AE, Fraanje J, Goubitz K, Schenk H, Rutjes FP, Hiemstra H.

J Org Chem. 2001 Jan 12;66(1):233-42.

PMID:
11429905
8.

A Raney-cobalt-mediated tandem reductive cyclization route to the 1,5-methanoazocino[4,3-b]indole framework of the uleine and Strychnos alkaloids.

Reekie TA, Banwell MG, Willis AC.

J Org Chem. 2012 Dec 7;77(23):10773-81. doi: 10.1021/jo302132d.

PMID:
23094681
9.

Total synthesis of (+)-sundiversifolide.

Yokoe H, Sasaki H, Yoshimura T, Shindo M, Yoshida M, Shishido K.

Org Lett. 2007 Mar 15;9(6):969-71.

PMID:
17295494
11.

Remarkably facile ring-size control in macrocyclization: synthesis of hemicucurbit[6]uril and hemicucurbit[12]uril.

Miyahara Y, Goto K, Oka M, Inazu T.

Angew Chem Int Ed Engl. 2004 Sep 27;43(38):5019-22. No abstract available.

PMID:
15384112
13.

Pressocucurbit[5]uril.

Ustrnul L, Kulhanek P, Lizal T, Sindelar V.

Org Lett. 2015 Feb 20;17(4):1022-5. doi: 10.1021/acs.orglett.5b00123.

PMID:
25654606
14.

Synthesis of substituted 1,4,5,6-tetrahydrocyclopenta[b]pyrroles by platinum-catalyzed cascade cyclization/ring expansion of 2-alkynyl-1-azaspiro[2.3]hexanes.

Yoshida M, Maeyama Y, Al-Amin M, Shishido K.

J Org Chem. 2011 Jul 15;76(14):5813-20. doi: 10.1021/jo201000f.

PMID:
21650194
15.

Construction of the benzylic quaternary carbon center of zoanthenol by intramolecular Mizoroki-Heck reaction of enone.

Hirai G, Koizumi Y, Moharram SM, Oguri H, Hirama M.

Org Lett. 2002 May 2;4(9):1627-30.

PMID:
11975645
17.

Synthesis of Strained 1,3-Diene Macrocycles via Copper-Mediated Castro-Stephens Coupling/Alkyne Reduction Tandem Reactions.

Li W, Schneider CM, Georg GI.

Org Lett. 2015 Aug 7;17(15):3902-5. doi: 10.1021/acs.orglett.5b01892.

PMID:
26176267
18.

Concise and stereocontrolled synthesis of the tetracyclic core of daphniglaucin C.

Hanessian S, Dorich S, Menz H.

Org Lett. 2013 Aug 16;15(16):4134-7. doi: 10.1021/ol4018112.

PMID:
23889206
19.

Gram scale synthesis of the C(18)-C(34) fragment of amphidinolide C.

Morra NA, Pagenkopf BL.

Org Lett. 2011 Feb 18;13(4):572-5. doi: 10.1021/ol1030074.

PMID:
21254755
20.

Synthesis of macrocyclic precursors of phomactins using [2,3]-Wittig rearrangements.

McGowan G, Thomas EJ.

Org Biomol Chem. 2009 Jun 21;7(12):2576-90. doi: 10.1039/b903256h.

PMID:
19503933
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