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Results: 1 to 20 of 104

1.

Stereospecific transformation of protected P-H group into P-O or P-N group in one-pot reaction.

Yao Q, Yuan C.

J Org Chem. 2012 Dec 7;77(23):10985-90. doi: 10.1021/jo302140q. Epub 2012 Nov 14.

PMID:
23121494
[PubMed - indexed for MEDLINE]
2.

Highly selective 1,4- and 1,6-addition of P(O)-H compounds to p-quinones: a divergent method for the synthesis of C- and O-phosphoryl hydroquinone derivatives.

Xiong B, Shen R, Goto M, Yin SF, Han LB.

Chemistry. 2012 Dec 21;18(52):16902-10. doi: 10.1002/chem.201202074. Epub 2012 Nov 9.

PMID:
23143865
[PubMed - indexed for MEDLINE]
3.

A synthetic study of chiral α-hydroxy-H-phosphinates based on proline catalysis.

Yao Q, Yuan C.

Chemistry. 2013 May 3;19(19):6080-8. doi: 10.1002/chem.201204195. Epub 2013 Mar 7.

PMID:
23471759
[PubMed - indexed for MEDLINE]
4.

Application of in situ silylation for improved, convenient preparation of fluorenylmethoxycarbonyl (Fmoc)-protected phosphinate amino acids.

Li S, Whitehead JK, Hammer RP.

J Org Chem. 2007 Apr 13;72(8):3116-8. Epub 2007 Mar 22. Erratum in: J Org Chem. 2007 Aug 3;72(16):6328.

PMID:
17375960
[PubMed - indexed for MEDLINE]
5.

Direct transformation of amides into α-amino phosphonates via a reductive phosphination process.

Gao Y, Huang Z, Zhuang R, Xu J, Zhang P, Tang G, Zhao Y.

Org Lett. 2013 Aug 16;15(16):4214-7. doi: 10.1021/ol4019419. Epub 2013 Aug 2.

PMID:
23909613
[PubMed - indexed for MEDLINE]
6.

Stereospecific halogenation of P(O)-H bonds with copper(II) chloride affording optically active Z1Z2P(O)Cl.

Zhou Y, Wang G, Saga Y, Shen R, Goto M, Zhao Y, Han LB.

J Org Chem. 2010 Nov 19;75(22):7924-7. doi: 10.1021/jo101540d. Epub 2010 Oct 29.

PMID:
21033680
[PubMed - indexed for MEDLINE]
8.

Copper-catalyzed oxidative cross-coupling of H-phosphonates and amides to N-acylphosphoramidates.

Jin X, Yamaguchi K, Mizuno N.

Org Lett. 2013 Jan 18;15(2):418-21. doi: 10.1021/ol303420g. Epub 2013 Jan 9.

PMID:
23302030
[PubMed - indexed for MEDLINE]
9.

Facile P,N-heterocycle synthesis via tandem aminomethylation-cyclization of H-phosphinate building blocks.

Queffélec C, Montchamp JL.

Org Biomol Chem. 2010 Jan 7;8(1):267-73. doi: 10.1039/b917428a. Epub 2009 Nov 5.

PMID:
20024158
[PubMed - indexed for MEDLINE]
10.

Synthesis of phosphonamidate peptides by Staudinger reactions of silylated phosphinic acids and esters.

Wilkening I, del Signore G, Hackenberger CP.

Chem Commun (Camb). 2011 Jan 7;47(1):349-51. doi: 10.1039/c0cc02472d. Epub 2010 Sep 7.

PMID:
20830364
[PubMed - indexed for MEDLINE]
11.

Stereospecific addition of H-P bond to alkenes: a simple method for the preparation of (R(P))-phenylphosphinates.

Han LB, Zhao CQ.

J Org Chem. 2005 Nov 25;70(24):10121-3.

PMID:
16292852
[PubMed - indexed for MEDLINE]
12.

Enantioselective synthesis of H-phosphinic acids bearing natural amino acid residues.

Yao Q, Yuan C.

J Org Chem. 2013 Jul 19;78(14):6962-74. doi: 10.1021/jo400798f. Epub 2013 Jul 2.

PMID:
23772951
[PubMed - indexed for MEDLINE]
13.

Asymmetric hydrogenation of enol phosphinates by iridium catalysts having N,P ligands.

Cheruku P, Gohil S, Andersson PG.

Org Lett. 2007 Apr 26;9(9):1659-61. Epub 2007 Mar 28.

PMID:
17388604
[PubMed - indexed for MEDLINE]
14.

Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase.

Mucha A, Lämmerhofer M, Lindner W, Pawełczak M, Kafarski P.

Bioorg Med Chem Lett. 2008 Mar 1;18(5):1550-4. doi: 10.1016/j.bmcl.2008.01.107. Epub 2008 Feb 2.

PMID:
18262419
[PubMed - indexed for MEDLINE]
15.

Stereospecific nucleophilic substitution of optically pure H-phosphinates: a general way for the preparation of chiral P-stereogenic phosphine oxides.

Xu Q, Zhao CQ, Han LB.

J Am Chem Soc. 2008 Sep 24;130(38):12648-55. doi: 10.1021/ja804412k. Epub 2008 Aug 30.

PMID:
18761459
[PubMed]
16.

Synthesis of phosphinopeptides via the Mannich ligation.

Li B, Cai S, Du DM, Xu J.

Org Lett. 2007 Jun 7;9(12):2257-60. Epub 2007 May 12.

PMID:
17497867
[PubMed - indexed for MEDLINE]
17.

Synthesis of P,N-heterocycles from omega-amino-H-phosphinates: conformationally restricted alpha-amino acid analogs.

Queffelec C, Ribière P, Montchamp JL.

J Org Chem. 2008 Nov 21;73(22):8987-91. doi: 10.1021/jo801768y. Epub 2008 Oct 15.

PMID:
18855477
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Highly enantioselective synthesis of beta-aminophosphinates with two stereogenic atoms and their conversion into optically pure ethyl beta-amino-H-phosphinates.

Zhang D, Yuan C.

Chemistry. 2009;15(16):4088-101. doi: 10.1002/chem.200802248.

PMID:
19241437
[PubMed - indexed for MEDLINE]
19.

Stereospecific coupling of H-phosphinates and secondary phosphine oxides with amines and alcohols: a general method for the preparation of optically active organophosphorus acid derivatives.

Wang G, Shen R, Xu Q, Goto M, Zhao Y, Han LB.

J Org Chem. 2010 Jun 4;75(11):3890-2. doi: 10.1021/jo100473s.

PMID:
20443613
[PubMed - indexed for MEDLINE]
20.

Highly efficient stereoconservative amidation and deamidation of alpha-amino acids.

Shendage DM, Fröhlich R, Haufe G.

Org Lett. 2004 Oct 14;6(21):3675-8.

PMID:
15469321
[PubMed - indexed for MEDLINE]

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