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Items: 1 to 20 of 99

1.

Bioinspired total synthesis of gymnothelignan N.

Li H, Zhang Y, Xie X, Ma H, Zhao C, Zhao G, She X.

Org Lett. 2014 Sep 5;16(17):4440-3. doi: 10.1021/ol501960j.

2.

Total synthesis of (-)-talaumidin and (-)-galbelgin.

Xue P, Wang LP, Jiao XZ, Jiang YJ, Xiao Q, Luo ZG, Xie P, Liang XT.

J Asian Nat Prod Res. 2009;11(3):281-7. doi: 10.1080/10286020802675191.

PMID:
19408154
3.

Regiodivergent synthesis of trisubstituted furans through Tf(2)O-catalyzed Friedel-Crafts acylation: a tool for access to tetrahydrofuran lignan analogues.

Comegna D, DellaGreca M, Rosaria Iesce M, Previtera L, Zarrelli A, Zuppolini S.

Org Biomol Chem. 2012 Feb 14;10(6):1219-24. doi: 10.1039/c1ob06560b.

PMID:
22179391
4.

Use of the benzyl mesylate for the synthesis of tetrahydrofuran lignan: syntheses of 7,8-trans, 7',8'-trans, 7,7'-cis, and 8,8'-cis-virgatusin stereoisomers.

Yamauchi S, Nakato T, Tsuchiya M, Akiyama K, Maruyama M, Sugahara T, Kishida T.

Biosci Biotechnol Biochem. 2007 Sep;71(9):2248-55.

5.

Enantioselective Synthesis of a Furan Lignan (+)-Sylvone.

Lee E, Bang J, Kwon J, Yu CM.

J Org Chem. 2015 Oct 16;80(20):10359-63. doi: 10.1021/acs.joc.5b01677.

PMID:
26414201
6.

First asymmetric synthesis of (-)-lintetralin via intramolecular Friedel-Crafts-type cyclization.

Enders D, Del Signore G, Berner OM.

Chirality. 2003 Jun;15(6):510-3.

PMID:
12774291
7.
8.

First enantioselective synthesis of (-)- and (+)-virgatusin, tetra-substituted tetrahydrofuran lignan.

Yamauchi S, Okazaki M, Akiyama K, Sugahara T, Kishida T, Kashiwagi T.

Org Biomol Chem. 2005 May 7;3(9):1670-5.

PMID:
15858648
9.

Enantioselective synthesis of the tetrahydrofuran lignans (-)- and (+)-magnolone.

Nakato T, Yamauchi S.

J Nat Prod. 2007 Oct;70(10):1588-92.

PMID:
17887723
10.
11.

Stereocontrolled syntheses of tetralone- and naphthyl-type lignans by a one-pot oxidative [3,3] rearrangement/Friedel-Crafts arylation.

Reddel JC, Lutz KE, Diagne AB, Thomson RJ.

Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1395-8. doi: 10.1002/anie.201307659.

PMID:
24356917
13.

Enantioselective total synthesis of the lignan (+)-linoxepin.

Tietze LF, Clerc J, Biller S, Duefert SC, Bischoff M.

Chemistry. 2014 Dec 15;20(51):17119-24. doi: 10.1002/chem.201404679.

PMID:
25345835
14.

Stereoselective synthesis of 3-alkyl-2-aryltetrahydrofuran-4-ols: total synthesis of (+/-)-paulownin.

Angle SR, Choi I, Tham FS.

J Org Chem. 2008 Aug 15;73(16):6268-78. doi: 10.1021/jo800901r.

PMID:
18646863
15.

Lignans from the aerial parts of Saururus chinensis: isolation, structural characterization, and their effects on platelet aggregation.

Tsai WJ, Shen CC, Tsai TH, Lin LC.

J Nat Prod. 2014 Jan 24;77(1):125-31. doi: 10.1021/np400772h.

PMID:
24387347
16.

Stereocontrolled total synthesis of hedyotol A.

Kawabe Y, Ishikawa R, Akao Y, Yoshida A, Inai M, Asakawa T, Hamashima Y, Kan T.

Org Lett. 2014 Apr 4;16(7):1976-9. doi: 10.1021/ol500524y.

PMID:
24660822
17.

Gymnothelignans A-O: conformation and absolute configuration analyses of lignans bearing tetrahydrofuran from Gymnotheca chinensis.

He D, Ding L, Xu H, Lei X, Xiao H, Zhou Y.

J Org Chem. 2012 Oct 5;77(19):8435-43. doi: 10.1021/jo301225v.

PMID:
22946788
19.

Synthesis of 3,4-dibenzyltetrahydrofuran lignans (9,9'-epoxylignanes).

Pohjoispää M, Wähälä K.

Molecules. 2013 Oct 24;18(11):13124-38. doi: 10.3390/molecules181113124. Review.

20.

Radical carboxyarylation approach to lignans. Total synthesis of (-)-arctigenin, (-)-matairesinol, and related natural products.

Fischer J, Reynolds AJ, Sharp LA, Sherburn MS.

Org Lett. 2004 Apr 29;6(9):1345-8.

PMID:
15101738
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