These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 17640021)

  • 1. Crossed-molecular-beam study on the formation of phenylacetylene from phenyl radicals and acetylene.
    Gu X; Zhang F; Guo Y; Kaiser RI
    Angew Chem Int Ed Engl; 2007; 46(36):6866-9. PubMed ID: 17640021
    [No Abstract]   [Full Text] [Related]  

  • 2. A crossed beams and ab initio investigation on the formation of cyanodiacetylene in the reaction of cyano radicals with diacetylene.
    Zhang F; Kim S; Kaiser RI; Jamal A; Mebel AM
    J Chem Phys; 2009 Jun; 130(23):234308. PubMed ID: 19548728
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The benzylidenecarbene-phenylacetylene rearrangement: an experimental and computational study.
    Moore KA; Vidaurri-Martinez JS; Thamattoor DM
    J Am Chem Soc; 2012 Dec; 134(49):20037-40. PubMed ID: 23176163
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymerization of phenylacetylene by rhodium complexes within a discrete space of apo-ferritin.
    Abe S; Hirata K; Ueno T; Morino K; Shimizu N; Yamamoto M; Takata M; Yashima E; Watanabe Y
    J Am Chem Soc; 2009 May; 131(20):6958-60. PubMed ID: 19453195
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Helical polymer brushes with a preferred-handed helix-sense triggered by a terminal optically active group in the pendant.
    Maeda K; Wakasone S; Shimomura K; Ikai T; Kanoh S
    Chem Commun (Camb); 2012 Apr; 48(27):3342-4. PubMed ID: 22363934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Topochemical polymerization of phenylacetylene macrocycles: a new strategy for the preparation of organic nanorods.
    Rondeau-Gagné S; Néabo JR; Desroches M; Larouche J; Brisson J; Morin JF
    J Am Chem Soc; 2013 Jan; 135(1):110-3. PubMed ID: 23249259
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Temperature-induced chiroptical changes in a helical poly(phenylacetylene) bearing N,N-diisopropylaminomethyl groups with chiral acids in water.
    Nagai K; Maeda K; Takeyama Y; Sato T; Yashima E
    Chem Asian J; 2007 Oct; 2(10):1314-21. PubMed ID: 17763496
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enantioselective addition of phenylacetylene to N-aryl arylimines catalyzed by Cu(II)-pyridine containing N-tosylatedaminoimine ligand complex.
    Liu B; Zhong Y; Li X
    Chirality; 2009 Jun; 21(6):595-9. PubMed ID: 18752285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathway for the stereocontrolled Z and E production of alpha,alpha-difluorine-substituted phenyl butenoates.
    Ghattas W; Hess CR; Iacazio G; Hardré R; Klinman JP; Réglier M
    J Org Chem; 2006 Oct; 71(22):8618-21. PubMed ID: 17064042
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of hydrogen abstraction acetylene addition mechanisms in the formation of chlorinated naphthalenes. 2. Kinetic modeling and the detailed mechanism of ring closure.
    McIntosh GJ; Russell DK
    J Phys Chem A; 2014 Dec; 118(51):12205-20. PubMed ID: 25420011
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hydrogen-bonded complexes of phenylacetylene with water, methanol, ammonia, and methylamine. The origin of methyl group-induced hydrogen bond switching.
    Sedlak R; Hobza P; Patwari GN
    J Phys Chem A; 2009 Jun; 113(24):6620-5. PubMed ID: 19514784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dithiafulvenyl-substituted phenylacetylene derivatives: synthesis and structure-property-reactivity relationships.
    Wang Y; Zhao Y
    Org Biomol Chem; 2015 Oct; 13(37):9575-9. PubMed ID: 26324780
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and Magnetic Properties of Stable Radical Derivatives Carrying a Phenylacetylene Unit.
    Miyashiro S; Ishii T; Miura Y; Yoshioka N
    Molecules; 2018 Feb; 23(2):. PubMed ID: 29425165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Using supercritical fluid chromatography to determine diffusion coefficients of 1,2-diethylbenzene, 1,4-diethylbenzene, 5-tert-butyl-m-xylene and phenylacetylene in supercritical carbon dioxide.
    Pizarro C; Suárez-Iglesias O; Medina I; Bueno JL
    J Chromatogr A; 2007 Oct; 1167(2):202-9. PubMed ID: 17850810
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Silver-catalyzed one-pot synthesis of arylnaphthalene lactones.
    Eghbali N; Eddy J; Anastas PT
    J Org Chem; 2008 Sep; 73(17):6932-5. PubMed ID: 18681406
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Macromolecular helicity inversion of an optically active helical poly(phenylacetylene) by chemical modification of the side groups.
    Kobayashi S; Morino K; Yashima E
    Chem Commun (Camb); 2007 Jun; (23):2351-3. PubMed ID: 17844743
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis and chiroptical properties of a helical poly(phenylacetylene) bearing optically active pyrene pendants.
    Lin H; Morino K; Yashima E
    Chirality; 2008 Mar; 20(3-4):386-92. PubMed ID: 17724655
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis and conformational analysis of poly(phenylacetylene)s with serinol-tethered carbohydrate appendages.
    Masubuchi K; Maehata M; Suzuki C; Matsuoka R; Sekiguchi M; Chigira N; Amano Y; Inokuchi M; Li Q; Hasegawa T
    Carbohydr Res; 2019 Jul; 481():23-30. PubMed ID: 31220628
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Electrochemical functionalization of carbon surfaces by aromatic azide or alkyne molecules: a versatile platform for click chemistry.
    Evrard D; Lambert F; Policar C; Balland V; Limoges B
    Chemistry; 2008; 14(30):9286-91. PubMed ID: 18780382
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Single-molecule phenyl-acetylene-macrocycle-based optoelectronic switch functioning as a quantum-interference-effect transistor.
    Hsu LY; Rabitz H
    Phys Rev Lett; 2012 Nov; 109(18):186801. PubMed ID: 23215309
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.