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Items: 1 to 20 of 98

1.

Highly regioselective ring-opening coupling of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents.

Cao J, Huang X, Wu L.

Chem Commun (Camb). 2013 May 25;49(42):4788-90. doi: 10.1039/c3cc00171g.

PMID:
23598448
2.

A ligand-controlled switch of regioselectivity in ring-opening coupling of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents.

Cao J, Huang X, Wu L.

Org Biomol Chem. 2016 Jan 14;14(2):729-37. doi: 10.1039/c3ob42084a.

PMID:
26579856
3.

Highly enantioselective copper-catalyzed ring opening of oxabicyclic alkenes with Grignard reagents.

Zhang W, Zhu SF, Qiao XC, Zhou QL.

Chem Asian J. 2008 Dec 1;3(12):2105-11. doi: 10.1002/asia.200800159.

PMID:
18823061
4.

Highly enantioselective Cu(I)-Tol-BINAP-catalyzed asymmetric conjugate addition of Grignard reagents to α,β-unsaturated esters.

Wang SY, Loh TP.

Chem Commun (Camb). 2010 Dec 14;46(46):8694-703. doi: 10.1039/c0cc03211e.

PMID:
21038042
5.

Iridium/Copper Co-catalyzed Anti-Stereoselective Ring Opening of Oxabenzonorbornadienes with Grignard Reagents.

Cheng G, Yang W, Li Y, Yang D.

J Org Chem. 2016 Sep 2;81(17):7817-23. doi: 10.1021/acs.joc.6b01479.

PMID:
27455165
6.

A Versatile Route to 2-Substituted Cyclic 1,3-Dienes via a Copper(I)-Catalyzed Cross-Coupling Reaction of Dienyl Triflates with Grignard Reagents.

Karlström AS, Rönn M, Thorarensen A, Bäckvall JE.

J Org Chem. 1998 Apr 17;63(8):2517-2522.

PMID:
11672113
7.

Titanocene-catalyzed regioselective alkylation of styrenes with grignard reagents using beta-bromoethyl ethers, thioethers, or amines.

Terao J, Kato Y, Kambe N.

Chem Asian J. 2008 Sep 1;3(8-9):1472-8. doi: 10.1002/asia.200800134.

PMID:
18613206
8.
10.

Highly versatile enantioselective conjugate addition of Grignard reagents to alpha,beta-unsaturated thioesters.

Ruiz BM, Geurts K, Fernández-Ibáñez MA, ter Horst B, Minnaard AJ, Feringa BL.

Org Lett. 2007 Nov 22;9(24):5123-6.

PMID:
17975924
11.

Copper-catalyzed anti-stereocontrolled ring-opening of azabicyclic alkenes with Grignard reagents.

Gómez Arrayás R, Cabrera S, Carretero JC.

Org Lett. 2005 Jan 20;7(2):219-21.

PMID:
15646962
12.

Copper-catalyzed asymmetric ring opening of oxabicyclic alkenes with Grignard reagents.

Zhang W, Wang LX, Shi WJ, Zhou QL.

J Org Chem. 2005 Apr 29;70(9):3734-6. Erratum in: J Org Chem. 2005 Jun 10;70(12):4902.

PMID:
15845018
13.

S(N)2 ring opening of beta-lactones: an alternative to catalytic asymmetric conjugate additions.

Nelson SG, Wan Z, Stan MA.

J Org Chem. 2002 Jul 12;67(14):4680-3.

PMID:
12098275
14.

Manganese(III) acetate-mediated cyclization of diarylmethylenecyclopropa[b]naphthalenes: a method for the synthesis of 1,2-benzanthracene derivatives.

Cao J, Miao M, Chen W, Wu L, Huang X.

J Org Chem. 2011 Nov 18;76(22):9329-37. doi: 10.1021/jo2015906.

PMID:
21992706
15.

Regioselective copper-catalyzed alkylation of [2.2.2]-acylnitroso cycloadducts: remarkable effect of the halide of Grignard reagents.

Crotti S, Bertolini F, di Bussolo V, Pineschi M.

Org Lett. 2010 Apr 16;12(8):1828-30. doi: 10.1021/ol100454c.

PMID:
20232855
16.

Nickel-catalyzed manipulation of tertiary phosphines via highly selective C-P bond cleavage.

Cao J, Huang X, Wu L.

Chem Commun (Camb). 2013 Sep 11;49(70):7747-9. doi: 10.1039/c3cc43640c.

PMID:
23882467
17.
18.

35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come?

Knappke CE, von Wangelin AJ.

Chem Soc Rev. 2011 Oct;40(10):4948-62. doi: 10.1039/c1cs15137a.

PMID:
21811712
19.

Synthesis of carboxylic amides by ring-opening of oxazolidinones with Grignard reagents.

Bensa D, Coldham I, Feinäugle P, Pathak RB, Butlin RJ.

Org Biomol Chem. 2008 Apr 21;6(8):1410-5. doi: 10.1039/b800849c.

PMID:
18385847
20.

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