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Items: 1 to 20 of 410

1.

Palladium-catalyzed regio-, diastereo-, and enantioselective allylation of nitroalkanes with monosubstituted allylic substrates.

Yang XF, Yu WH, Ding CH, Ding QP, Wan SL, Hou XL, Dai LX, Wang PJ.

J Org Chem. 2013 Jul 5;78(13):6503-9. doi: 10.1021/jo400663d. Epub 2013 Jun 24.

PMID:
23741970
2.

Regio- and enantioselective palladium-catalyzed allylic alkylation of nitromethane with monosubstituted allyl substrates: synthesis of (R)-rolipram and (R)-baclofen.

Yang XF, Ding CH, Li XH, Huang JQ, Hou XL, Dai LX, Wang PJ.

J Org Chem. 2012 Oct 19;77(20):8980-5. doi: 10.1021/jo301506p. Epub 2012 Oct 1.

PMID:
22992268
3.

Pd-catalyzed highly regio-, diastereo-, and enantioselective allylic alkylation of α-fluorophosphonates.

Huang Y, Zhang QS, Fang P, Chen TG, Zhu J, Hou XL.

Chem Commun (Camb). 2014 Jun 28;50(51):6751-3. doi: 10.1039/c4cc02158d.

PMID:
24831029
4.

Palladium- or iridium-catalyzed allylic substitution of guanidines: convenient and direct modification of guanidines.

Miyabe H, Yoshida K, Reddy VK, Takemoto Y.

J Org Chem. 2009 Jan 2;74(1):305-11. doi: 10.1021/jo802271d.

PMID:
19053613
5.

Enantioselective synthesis of 2,3-disubstituted indanones via Pd-catalyzed intramolecular asymmetric allylic alkylation of ketones.

Li XH, Zheng BH, Ding CH, Hou XL.

Org Lett. 2013 Dec 6;15(23):6086-9. doi: 10.1021/ol402980v. Epub 2013 Nov 8.

PMID:
24206052
6.

Pd-catalyzed asymmetric allylic alkylation of pyrazol-5-ones with allylic alcohols: the role of the chiral phosphoric acid in C-O bond cleavage and stereocontrol.

Tao ZL, Zhang WQ, Chen DF, Adele A, Gong LZ.

J Am Chem Soc. 2013 Jun 26;135(25):9255-8. doi: 10.1021/ja402740q. Epub 2013 Jun 14.

PMID:
23734612
7.
8.

Selective peptide modifications via ruthenium-catalyzed allylic alkylations.

Bayer A, Kazmaier U.

J Org Chem. 2014 Sep 5;79(17):8491-7. doi: 10.1021/jo501731y. Epub 2014 Aug 21.

PMID:
25118961
9.

Catalytic intermolecular allylic C-H alkylation.

Young AJ, White MC.

J Am Chem Soc. 2008 Oct 29;130(43):14090-1. doi: 10.1021/ja806867p. Epub 2008 Oct 3.

PMID:
18831588
10.

Hydrogen-Bond Directed Regioselective Pd-Catalyzed Asymmetric Allylic Alkylation: The Construction of Chiral α-Amino Acids with Vicinal Tertiary and Quaternary Stereocenters.

Wei X, Liu D, An Q, Zhang W.

Org Lett. 2015 Dec 4;17(23):5768-71. doi: 10.1021/acs.orglett.5b02868. Epub 2015 Nov 17.

PMID:
26575242
11.
12.

Pd(II)/Brønsted acid catalyzed enantioselective allylic C-H activation for the synthesis of spirocyclic rings.

Chai Z, Rainey TJ.

J Am Chem Soc. 2012 Feb 29;134(8):3615-8. doi: 10.1021/ja2102407. Epub 2012 Feb 17.

PMID:
22313246
13.

Direct asymmetric α-allylation of α-branched aldehydes by two catalytic systems with an achiral Pd complex and a chiral primary α-amino acid.

Yoshida M, Terumine T, Masaki E, Hara S.

J Org Chem. 2013 Nov 1;78(21):10853-9. doi: 10.1021/jo4018414. Epub 2013 Oct 21.

PMID:
24102624
14.

Chemoselective palladium-catalyzed α-allylation of α-boryl aldehydes.

St Denis JD, He Z, Yudin AK.

Org Biomol Chem. 2012 Oct 21;10(39):7900-2.

PMID:
22911058
16.

Enantioselective synthesis of α-quaternary Mannich adducts by palladium-catalyzed allylic alkylation: total synthesis of (+)-sibirinine.

Numajiri Y, Pritchett BP, Chiyoda K, Stoltz BM.

J Am Chem Soc. 2015 Jan 28;137(3):1040-3. doi: 10.1021/ja512124c. Epub 2015 Jan 20.

17.

Palladium-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of acylsilanes with monosubstituted allyl substrates.

Chen JP, Ding CH, Liu W, Hou XL, Dai LX.

J Am Chem Soc. 2010 Nov 10;132(44):15493-5. doi: 10.1021/ja106703y.

PMID:
20945898
18.
19.

Copper-catalyzed divergent kinetic resolution of racemic allylic substrates.

Pineschi M, Di Bussolo V, Crotti P.

Chirality. 2011 Oct;23(9):703-10. doi: 10.1002/chir.20980. Epub 2011 Aug 12. Review.

PMID:
21837639
20.

Z-Selective copper-catalyzed asymmetric allylic alkylation with Grignard reagents.

Giannerini M, Fañanás-Mastral M, Feringa BL.

J Am Chem Soc. 2012 Mar 7;134(9):4108-11. doi: 10.1021/ja300743t. Epub 2012 Feb 27.

PMID:
22352853

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