Synthesis, Inhaltsverzeichnis PAPER© Georg Thieme Verlag Stuttgart ˙ New YorkSynthesis of Extended Bifunctional TriptycenesJiří Rybáček, Jiří Závada, Petr Holý*Institute of Organic Chemistry and Biochemistry, v.v.i., Academy of Sciences of the Czech Republic, Flemingovo n. 2., 166 10 Prague 6, Czech RepublicFax: +420(2)20183560; e-Mail: petrholy@uochb.cas.cz; Artikel empfehlen Abstract Artikel einzeln kaufen Alle Artikel dieser Rubrik Abstract Extended triptycenes 5a,b and 7a-c have been designed to serve as convenient building blocks for a stepwise ramification of the parent triptycene structure by Diels-Alder oligomerization. Key words anthracenes - arynes - Diels-Alder reaction - quinones - triptycenes Volltext Referenzen References <A NAME="RT10708SS-1">1</A> Godinez CE. Zepeda G. Mortko CJ. Dang H. Garcia-Garibay MA. J. Org. Chem. 2004, 69: 1652 <A NAME="RT10708SS-2">2</A> Caskey DC. Wang B. Zheng X. Michl J. Collect. Czech. Chem. Commun. 2005, 70: 1970 <A NAME="RT10708SS-3">3</A> Kelly TR. DeSilva H. Silva RA. Nature 1999, 401: 150 <A NAME="RT10708SS-4A">4a</A> Rybáček J. Rybáčková M. Høj M. Bělohradský M. Holý P. Kilså K. Nielsen MB. Tetrahedron 2007, 63: 8840 <A NAME="RT10708SS-4B">4b</A> Rybáčková M. Bělohradský M. Holý P. Pohl R. Dekoj V. Závada J. Synthesis 2007, 1554 <A NAME="RT10708SS-5A">5a</A> Hart H. Bashir-Hashemi A. Luo J. Meador MA. Tetrahedron 1986, 42: 1641 <A NAME="RT10708SS-5B">5b</A> Hart H. Pure Appl. Chem. 1993, 65: 27 <A NAME="RT10708SS-6">6</A> Thomas SW. Long TM. Pate BD. Kline SR. Thomas EL. Swager TM. J. Am. Chem. Soc. 2005, 127: 17976 <A NAME="RT10708SS-7">7</A> Hart H. Lai C.-Y. Nwokogu GC. Shamouilian S. Tetrahedron 1987, 43: 5203 <A NAME="RT10708SS-8">8</A> Peyton J. Callery PS. Shulgin AT. Castagnoli N. J. Org. Chem. 1976, 41: 3627 <A NAME="RT10708SS-9">9</A> Lin C.-T. Chou T.-C. Synthesis 1988, 628 <A NAME="RT10708SS-10">10</A> Zimmerman HE. Amick DR. J. Am. Chem. Soc. 1973, 95: 3977 <A NAME="RT10708SS-11">11</A> Wiehe A. Senge MO. Kurreck H. Liebigs Ann./Recl. 1997, 1951 <A NAME="RT10708SS-12">12</A> Koreeda M. Gopalaswamy R. J. Am. Chem. Soc. 1995, 117: 10595 <A NAME="RT10708SS-13">13</A> LeHoullier CS. Gribble GW. J. Org. Chem. 1983, 48: 2364 <A NAME="RT10708SS-14">14</A> Kitamura T. Fukatsu N. Fujiwara Y. J. Org. Chem. 1998, 63: 8579 <A NAME="RT10708SS-15">15</A> Zhu X.-Z. Chen C.-F. J. Org. Chem. 2005, 70: 917 <A NAME="RT10708SS-16">16</A> Quast H. Fuchsbauer H.-L. Chem. Ber. 1986, 119: 1016 <A NAME="RT10708SS-17">17</A> Hua DH. Tamura M. Huang X. Stephany HA. Helfrich BA. Perchellet EM. Sperfslage BJ. Perchellet J.-P. Jiang S. Kyle DE. Chiang PK. J. Org. Chem. 2002, 67: 2907 <A NAME="RT10708SS-18">18</A> Raw AS. Jang EB. Tetrahedron 2000, 56: 3285