Aromatic Thioesters as Protecting Groups for Thiols Against 1,2‐Didehydrobenzenes
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A. Terfort | Andreas Terfort | Christian Fowelin | B. Schüpbach | Björn Schüpbach | Christian Fowelin | Björn Schüpbach
[1] Q. Zong,et al. Novel triptycene-based cylindrical macrotricyclic host: synthesis and complexation with paraquat derivatives. , 2006, Organic letters.
[2] T R Kelly,et al. Progress toward a rationally designed molecular motor. , 2001, Accounts of chemical research.
[3] E. Ciganek. Intramolecular Diels-Alder additions. 1. Additions to anthracene and acridine , 1980 .
[4] G. Wittig,et al. Über lithium‐natrium‐organische Komplexe, III. Über Anionisierungsreaktionen mit Diphenyl‐lithium‐natrium , 1958 .
[5] D. Fitzmaurice,et al. Heterosupramolecular Chemistry: An Approach to Modulating Function in Molecular Devices , 1996 .
[6] L. Mao,et al. Rational attachment of synthetic triptycene orthoquinone onto carbon nanotubes for electrocatalysis and sensitive detection of thiols. , 2005, Analytical chemistry.
[7] T. Aida,et al. Toward intelligent molecular machines: directed motions of biological and artificial molecules and assemblies. , 2005, Chemical reviews.
[8] T. Ross Kelly,et al. New Molecular Devices: In Search of a Molecular Ratchet , 1998 .
[9] Gosch,et al. Protecting Groups for Thiols Suitable for Suzuki Conditions. , 2000, Organic letters.
[10] J. F. Stoddart,et al. Building supramolecular nanostructures on surfaces: the influence of the substrate , 1997 .
[11] O. Nishimura,et al. New method for removing the S-p-methoxybenzyl and S-t-butyl groups of cysteine residues with mercuric trifluoroacetate. , 1978 .
[12] Y. Shimonishi,et al. Use of anhydrous hydrogen fluoride in peptide synthesis. I. Behavior of various protective groups in anhydrous hydrogen fluoride. , 1967, Bulletin of the Chemical Society of Japan.
[13] Chuan-feng Chen,et al. A highly efficient approach to [4]pseudocatenanes by threefold metathesis reactions of a triptycene-based tris[2]pseudorotaxane. , 2005, Journal of the American Chemical Society.
[14] L. Friedman,et al. Arynes via aprotic diazotization of anthranilic acids , 1969 .
[15] L. Friedman,et al. Benzynes via Aprotic Diazotization of Anthranilic Acids: A Convenient Synthesis of Triptycene and Derivatives , 1963 .
[16] Ben L. Feringa,et al. Unidirectional molecular motor on a gold surface , 2005, Nature.
[17] T. Kitamura,et al. Synthesis, Solubility, and Reaction of Long Alkyl-Chained Hypervalent Iodine Benzyne Precursors , 2003 .
[18] R. Sachleben,et al. Molecular gears: Structures of (9,10-triptyceno) crown ethers , 1999 .
[19] Richard A. Silva,et al. Unidirectional rotary motion in a molecular system , 1999, Nature.
[20] T. Criswell,et al. Reactivity of benzyne toward anthracene systems , 1969 .
[21] S. Huang,et al. Rearrangement and Cleavage of 2-Aryliodoniobenzoates. Trapping Agents for Benzyne1-3 , 1964 .
[22] R. Pannier,et al. Über Ferrocenderivate. VIII. Die Darstellung von monomeren und polymeren Ferrocenylenoxadiazolen , 1967 .
[23] G. W. Anderson,et al. The Tertiary Butyl Group as a Blocking Agent for Hydroxyl, Sulfhydryl and Amido Functions in Peptide Synthesis , 1963 .
[24] J. Michl,et al. Self-Assembled Trigonal Prismatic Altitudinal Rotors with Triptycene Paddle Wheels , 2005 .
[25] Hiroshi Kobayashi,et al. FLUORIDE-INDUCED 1,2-ELIMINATION OF O-TRIMETHYLSILYLPHENYL TRIFLATE TO BENZYNE UNDER MILD CONDITIONS , 1983 .