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Items: 1 to 20 of 135

1.

Diastereoselective synthesis of vicinal cis-dihydroxyheterospirocycles by one-pot epoxidation/spirocyclization of C(3)-functionalized cyclohex-2-en-1-ols.

Yeh MC, Liang CJ, Liu CY, Shih YF, Lee IC, Liu HF, Wang JL.

Org Biomol Chem. 2013 May 28;11(20):3393-9. doi: 10.1039/c3ob27352k.

PMID:
23563191
2.

Synthesis of 2-azaspiro[4.6]undec-7-enes from N-tosyl-N-(3-arylpropargyl)-tethered 3-methylcyclohex-2-en-1-ols.

Yeh MC, Liang CJ, Fan CW, Chiu WH, Lo JY.

J Org Chem. 2012 Nov 2;77(21):9707-17. doi: 10.1021/jo301764g.

PMID:
23075326
3.

Straightforward stereoselective synthesis of spiro-epoxyoxindoles.

Schulz V, Davoust M, Lemarié M, Lohier JF, Santos JS, Metzner P, Brière JF.

Org Lett. 2007 Apr 26;9(9):1745-8.

PMID:
17394349
4.

Enantio- and diastereoselective synthesis of spiro-epoxyoxindoles.

Boucherif A, Yang QQ, Wang Q, Chen JR, Lu LQ, Xiao WJ.

J Org Chem. 2014 May 2;79(9):3924-9. doi: 10.1021/jo5003856.

PMID:
24730463
5.

Total syntheses of the assigned structures of lituarines B and C.

Smith AB 3rd, Duffey MO, Basu K, Walsh SP, Suennemann HW, Frohn M.

J Am Chem Soc. 2008 Jan 16;130(2):422-3. No abstract available.

PMID:
18095694
6.

Noncovalent organocatalysis: a powerful tool for the nucleophilic epoxidation of α-ylideneoxindoles.

Palumbo C, Mazzeo G, Mazziotta A, Gambacorta A, Loreto MA, Migliorini A, Superchi S, Tofani D, Gasperi T.

Org Lett. 2011 Dec 2;13(23):6248-51. doi: 10.1021/ol202646w.

PMID:
22053986
7.

Lituarine synthetic studies. An efficient, stereocontrolled construction of the common c(7-19) tricyclic spiroketal fragment.

Smith AB 3rd, Frohn M.

Org Lett. 2001 Nov 29;3(24):3979-82. Erratum in: Org Lett 2002 Nov 14;4(23):4183.

PMID:
11720584
8.

A diversity-oriented approach to spiroindolines: post-Ugi gold-catalyzed diastereoselective domino cyclization.

Modha SG, Kumar A, Vachhani DD, Jacobs J, Sharma SK, Parmar VS, Van Meervelt L, Van der Eycken EV.

Angew Chem Int Ed Engl. 2012 Sep 17;51(38):9572-5. doi: 10.1002/anie.201205052. No abstract available.

PMID:
22907654
9.

A highly enantioselective one-pot synthesis of spirolactones by an organocatalyzed Michael addition/cyclization sequence.

Sternativo S, Calandriello A, Costantino F, Testaferri L, Tiecco M, Marini F.

Angew Chem Int Ed Engl. 2011 Sep 26;50(40):9382-5. doi: 10.1002/anie.201104819. No abstract available.

PMID:
21858906
11.
12.

Highly enantio- and diastereoselective one-pot synthesis of acyclic epoxy alcohols with three contiguous stereocenters.

Lurain AE, Maestri A, Kelly AR, Carroll PJ, Walsh PJ.

J Am Chem Soc. 2004 Oct 27;126(42):13608-9.

PMID:
15493905
13.

Synthesis of a functionalized 7,6-bicyclic spiroimine ring fragment of the spirolides.

Guéret SM, Furkert DP, Brimble MA.

Org Lett. 2010 Nov 19;12(22):5226-9. doi: 10.1021/ol102525w.

PMID:
21028788
14.

Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol.

Krief A, Gondal HY, Kremer A.

Chem Commun (Camb). 2008 Oct 21;(39):4753-5. doi: 10.1039/b808695h.

PMID:
18830482
15.
16.

One-pot tandem double-aldol reaction/aza-addition of acetylacetamides and o-phthalaldehyde leading to spiroindan-2,2'-pyrrolidines.

Cheng X, Liang F, Shi F, Zhang L, Liu Q.

Org Lett. 2009 Jan 1;11(1):93-6. doi: 10.1021/ol802507y.

PMID:
19035841
17.
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19.

Formal total synthesis of (+)-diepoxin sigma.

Wipf P, Jung JK.

J Org Chem. 2000 Oct 6;65(20):6319-37.

PMID:
11052073
20.
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