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Results: 1 to 20 of 207

1.

Reductive coupling of terpenic allylic halides catalyzed by Cp2TiCl: a short and efficient asymmetric synthesis of onocerane triterpenes.

Barrero AF, Herrador MM, Quílez del Moral JF, Arteaga P, Arteaga JF, Piedra M, Sánchez EM.

Org Lett. 2005 Jun 9;7(12):2301-4.

PMID:
15932183
[PubMed - indexed for MEDLINE]
2.

Mild TiIII- and Mn/ZrIV-catalytic reductive coupling of allylic halides: efficient synthesis of symmetric terpenes.

Barrero AF, Herrador MM, del Moral JF, Arteaga P, Arteaga JF, Diéguez HR, Sánchez EM.

J Org Chem. 2007 Apr 13;72(8):2988-95. Epub 2007 Mar 22.

PMID:
17375959
[PubMed - indexed for MEDLINE]
3.

Palladium-catalyzed three-component coupling of arynes with allylic acetates or halides and terminal alkynes promoted by cuprous iodide.

Bhuvaneswari S, Jeganmohan M, Yang MC, Cheng CH.

Chem Commun (Camb). 2008 May 14;(18):2158-60. doi: 10.1039/b800118a. Epub 2008 Mar 3.

PMID:
18438501
[PubMed - indexed for MEDLINE]
4.

Asymmetric synthesis of highly substituted gamma-amino acids from allyltitanium sulfoximines.

Köhler F, Gais HJ, Raabe G.

Org Lett. 2007 Mar 29;9(7):1231-4. Epub 2007 Feb 28.

PMID:
17326643
[PubMed - indexed for MEDLINE]
5.

Solid-phase selenium-catalyzed selective allylic chlorination of polyprenoids: facile syntheses of biologically active terpenoids.

Barrero AF, Quílez Del Moral JF, Herrador MM, Cortés M, Arteaga P, Catalan JV, Sanchez EM, Arteaga JF.

J Org Chem. 2006 Jul 21;71(15):5811-4.

PMID:
16839173
[PubMed - indexed for MEDLINE]
6.

Palladium-catalyzed cross-coupling between vinyl halides and tert-butyl carbazate: first general synthesis of the unusual N-Boc-N-alkenylhydrazines.

Barluenga J, Moriel P, Aznar F, Valdés C.

Org Lett. 2007 Jan 18;9(2):275-8.

PMID:
17217283
[PubMed - indexed for MEDLINE]
8.

Efficient synthesis of sterically crowded biaryls by palladium-phosphinous acid-catalyzed cross-coupling of aryl halides and aryl grignards.

Wolf C, Xu H.

J Org Chem. 2008 Jan 4;73(1):162-7. Epub 2007 Dec 6.

PMID:
18052388
[PubMed - indexed for MEDLINE]
9.

High diversity on simple substrates: 1,4-dihalo-2-butenes and other difunctionalized allylic halides for copper-catalyzed S(N)2' reactions.

Falciola CA, Alexakis A.

Chemistry. 2008;14(34):10615-27. doi: 10.1002/chem.200801309.

PMID:
18924190
[PubMed - indexed for MEDLINE]
10.

Nickel-catalyzed cross-coupling reaction of alkyl halides with organozinc and Grignard reagents with 1,3,8,10-tetraenes as additives.

Terao J, Todo H, Watanabe H, Ikumi A, Kambe N.

Angew Chem Int Ed Engl. 2004 Nov 19;43(45):6180-2. No abstract available.

PMID:
15549748
[PubMed - indexed for MEDLINE]
11.

Control of skeletal connectivity in indium promoted reactions: 1,2-additions and cope rearrangements en route to lactol formation.

Mitzel T, Wzorek J, Troutman A, Allegue K.

J Org Chem. 2007 Apr 13;72(8):3042-52. Epub 2007 Mar 10.

PMID:
17348712
[PubMed - indexed for MEDLINE]
13.
14.

Reductive alkylation of beta-alkoxy aziridines: new route to substituted allylic amines.

Rosser CM, Coote SC, Kirby JP, O'Brien P, Caine D.

Org Lett. 2004 Dec 23;6(26):4817-9.

PMID:
15606074
[PubMed - indexed for MEDLINE]
15.

Nickel-catalyzed reductive cross-coupling of aryl halides with alkyl halides.

Everson DA, Shrestha R, Weix DJ.

J Am Chem Soc. 2010 Jan 27;132(3):920-1. doi: 10.1021/ja9093956. Erratum in: J Am Chem Soc. 2010 Mar 17;132(10):3636.

PMID:
20047282
[PubMed - indexed for MEDLINE]
17.

Nickel-catalyzed thioallylation of alkynes with allyl phenyl sulfides.

Hua R, Takeda H, Onozawa SY, Abe Y, Tanaka M.

Org Lett. 2007 Jan 18;9(2):263-6.

PMID:
17217280
[PubMed - indexed for MEDLINE]
18.

Atom transfer cyclization catalyzed by InCl3 via halogen activation.

Cook GR, Hayashi R.

Org Lett. 2006 Mar 16;8(6):1045-8.

PMID:
16524264
[PubMed - indexed for MEDLINE]
19.

Hydroxylamines as oxygen atom nucleophiles in transition-metal-catalyzed allylic substitution.

Miyabe H, Yoshida K, Yamauchi M, Takemoto Y.

J Org Chem. 2005 Mar 18;70(6):2148-53.

PMID:
15760199
[PubMed - indexed for MEDLINE]
20.

Palladium-catalyzed allylation of acidic and less nucleophilic anilines using allylic alcohols directly.

Hsu YC, Gan KH, Yang SC.

Chem Pharm Bull (Tokyo). 2005 Oct;53(10):1266-9.

PMID:
16204982
[PubMed - indexed for MEDLINE]
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