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Items: 1 to 20 of 94

1.

Tribenzotriquinacene: a versatile synthesis and C3-chiral platforms.

Markopoulos G, Henneicke L, Shen J, Okamoto Y, Jones PG, Hopf H.

Angew Chem Int Ed Engl. 2012 Dec 14;51(51):12884-7. doi: 10.1002/anie.201207220. Epub 2012 Nov 9. No abstract available.

PMID:
23144000
2.

Solid-state enantiopure organic nanocubes formed by self organization of a C3-symmetrical tribenzotriquinacene.

Strübe J, Neumann B, Stammler HG, Kuck D.

Chemistry. 2009;15(10):2256-60. doi: 10.1002/chem.200802371.

PMID:
19191245
3.
5.

Advanced buckyball joints: synthesis, complex formation and computational simulations of centrohexaindane-extended tribenzotriquinacene receptors for C60 fullerene.

Henne S, Bredenkötter B, Dehghan Baghi AA, Schmid R, Volkmer D.

Dalton Trans. 2012 May 21;41(19):5995-6002. doi: 10.1039/c2dt12435a. Epub 2012 Apr 5.

PMID:
22476453
6.

[Efficient chiral control based on five-membered heterocyclic and related systems].

Kunieda T.

Yakugaku Zasshi. 2000 Dec;120(12):1323-35. Review. Japanese.

PMID:
11193382
7.

TADDOLs, Their Derivatives, and TADDOL Analogues: Versatile Chiral Auxiliaries.

Seebach D, Beck AK, Heckel A.

Angew Chem Int Ed Engl. 2001 Jan 5;40(1):92-138.

PMID:
11169693
8.

Practical chiral alcohol manufacture using ketoreductases.

Huisman GW, Liang J, Krebber A.

Curr Opin Chem Biol. 2010 Apr;14(2):122-9. doi: 10.1016/j.cbpa.2009.12.003. Epub 2010 Jan 12. Review.

PMID:
20071211
10.

Organocatalytic tandem reaction to construct six-membered spirocyclic oxindoles with multiple chiral centres through a formal [2+2+2] annulation.

Jiang K, Jia ZJ, Chen S, Wu L, Chen YC.

Chemistry. 2010 Mar 1;16(9):2852-6. doi: 10.1002/chem.200903009.

PMID:
20112315
11.

Synthesis and applications of novel, highly efficient HPLC chiral stationary phases: a chiral dimension in drug research analysis.

Cancelliere G, D'Acquarica I I, Gasparrini F, Misiti D, Villani C.

Pharm Sci Technolo Today. 1999 Dec;2(12):484-492.

PMID:
10603466
12.
13.

Production of chiral C3- and C4-units by microbial enzymes.

Shimizu S, Kataoka M.

Adv Biochem Eng Biotechnol. 1999;63:109-23.

PMID:
9933983
14.

A sensitivity-enhanced field-effect chiral sensor.

Torsi L, Farinola GM, Marinelli F, Tanese MC, Omar OH, Valli L, Babudri F, Palmisano F, Zambonin PG, Naso F.

Nat Mater. 2008 May;7(5):412-7. doi: 10.1038/nmat2167. Epub 2008 Apr 20.

PMID:
18425136
15.
16.

Versatile synthesis of the C3-C14 domain of 7-deoxyokadaic acid.

Trygstad TM, Pang Y, Forsyth CJ.

J Org Chem. 2009 Jan 16;74(2):910-3. doi: 10.1021/jo8017457.

PMID:
19072579
18.

Synthesis and chiroptical properties of chiral azoaromatic dendrimers with a C3-symmetrical core.

Angiolini L, Benelli T, Giorgini L.

Chirality. 2010 Jan;22(1):99-109. doi: 10.1002/chir.20712.

PMID:
19387991
19.

Catalytic asymmetric conjugate addition of Grignard reagents to coumarins--synthesis of versatile chiral building blocks.

Teichert JF, Feringa BL.

Chem Commun (Camb). 2011 Mar 7;47(9):2679-81. doi: 10.1039/c0cc05160h. Epub 2011 Jan 31.

PMID:
21279221
20.

Single-wing extended tribenzotriquinacenes via bowl-shaped dehydrobenzene and isobenzofuran tribenzotriquinacene derivatives.

Niu WX, Yang EQ, Shi ZF, Cao XP, Kuck D.

J Org Chem. 2012 Feb 3;77(3):1422-34. doi: 10.1021/jo2022668. Epub 2012 Jan 12.

PMID:
22148679
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