The New Inductees in the “Hall of Phane”—No Phane, No Gain
- 1 October 1996
- journal article
- highlight
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 35 (18) , 2085-2088
- https://doi.org/10.1002/anie.199620851
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Dioxa[8](2,7)pyrenophan, ein stark verzerrter, polycyclischer, aromatischer KohlenwasserstoffAngewandte Chemie, 1996
- Precursors to Endohedral Metal Fullerene Complexes: Synthesis and X-ray Structure of a Flexible Acetylenic Cyclophane C60H18Journal of the American Chemical Society, 1996
- Ein „molekulares Schaufelrad”︁: [3.3.3.3.3.3](1, 2, 3, 4, 5, 6)CyclophanAngewandte Chemie, 1996
- 6,7‐Bis(methoxycarbonyl)‐2,3‐dimethyl‐[5](1,4)naphthalinophan, das erste benzoanellierte [5]ParacyclophanAngewandte Chemie, 1995
- Synthesis and Conformational Analysis of 3,3,12,12-Tetramethyl[4.4]paracyclophane-2,13-dioneThe Journal of Organic Chemistry, 1995
- Multibridged [3n]Cyclophanes, 1. Synthesis of [34](1,2,3,5)‐ and ‐(1,2,4,5)CyclophanesEuropean Journal of Inorganic Chemistry, 1993
- Synthesis, molecular structure, and properties of in-phosphaphanes with substituted basal aromatic ringsThe Journal of Organic Chemistry, 1993
- in-Cyclophanes containing second-row elements poised above aromatic ringsJournal of the American Chemical Society, 1991
- Synthesis of in-[34,10][7]metacyclophane: projection of an aliphatic hydrogen toward the center of an aromatic ringJournal of the American Chemical Society, 1987
- A comment on the structure and proton NMR spectrum of 2,8,17-trithia[45,12][9]metacyclophaneThe Journal of Organic Chemistry, 1987