-
2
-
-
24544442181
-
Eine neue Generation chiraler Trennphasen für die Gaschromatographie
-
(a) König, W.A. Eine neue Generation chiraler Trennphasen für die Gaschromatographie. Nachr. Chem. Tech. Lab. 37:471-476, 1989;
-
(1989)
Nachr. Chem. Tech. Lab.
, vol.37
, pp. 471-476
-
-
König, W.A.1
-
3
-
-
0000367353
-
Gaschromatographische Enantiomerentrennung an Cyclodextrinderivaten
-
(b) Schurig, V., Nowotny, H.-P. Gaschromatographische Enantiomerentrennung an Cyclodextrinderivaten. Angew. Chem. 102:969-986, 1990; Angew. Chem. Int. Ed. Engl. 29:939-956, 1990.
-
(1990)
Angew. Chem.
, vol.102
, pp. 969-986
-
-
Schurig, V.1
Nowotny, H.-P.2
-
4
-
-
0025006411
-
-
(b) Schurig, V., Nowotny, H.-P. Gaschromatographische Enantiomerentrennung an Cyclodextrinderivaten. Angew. Chem. 102:969-986, 1990; Angew. Chem. Int. Ed. Engl. 29:939-956, 1990.
-
(1990)
Angew. Chem. Int. Ed. Engl.
, vol.29
, pp. 939-956
-
-
-
5
-
-
12044259565
-
Enantioselective and diastereoselective molecular recognition of neutral molecules
-
(a) Webb, T.H., Wilcox, C.S. Enantioselective and diastereoselective molecular recognition of neutral molecules. Chem. Soc. Rev. 383-395, 1993.
-
(1993)
Chem. Soc. Rev.
, pp. 383-395
-
-
Webb, T.H.1
Wilcox, C.S.2
-
6
-
-
0001332950
-
Destillative Racematspaltung mit Hilfe von Einschlußverbindungen
-
(b) Kaupp, G. Destillative Racematspaltung mit Hilfe von Einschlußverbindungen. Angew. Chem. 106:768-770, 1994; Angew. Chem. Int. Ed. Engl. 33:728-730, 1994.
-
(1994)
Angew. Chem.
, vol.106
, pp. 768-770
-
-
Kaupp, G.1
-
7
-
-
33748224273
-
-
(b) Kaupp, G. Destillative Racematspaltung mit Hilfe von Einschlußverbindungen. Angew. Chem. 106:768-770, 1994; Angew. Chem. Int. Ed. Engl. 33:728-730, 1994.
-
(1994)
Angew. Chem. Int. Ed. Engl.
, vol.33
, pp. 728-730
-
-
-
8
-
-
0003325128
-
Molecular Inclusion and Molecular Recognition: Clathrates I and II
-
Berlin-Heidelberg: Springer
-
(a) Weber, E., ed. Molecular Inclusion and Molecular Recognition: Clathrates I and II. Topics in Current Chemistry, Vols. 140 and 149. Berlin-Heidelberg: Springer, 1987, 1988.
-
(1987)
Topics in Current Chemistry
, vol.140-149
-
-
Weber, E.1
-
9
-
-
0002721724
-
Solid state Supramolecular Chemistry: Crystal Engineering
-
Oxford: Elsevier
-
(b) MacNicol, D.D., Toda, F., Bishop, R., eds. Solid state Supramolecular Chemistry: Crystal Engineering. Comprehensive Supramolecular Chemistry. Vol. 6. Oxford: Elsevier, 1996.
-
(1996)
Comprehensive Supramolecular Chemistry
, vol.6
-
-
MacNicol, D.D.1
Toda, F.2
Bishop, R.3
-
10
-
-
0000741239
-
Inclusion by acetylenic alcohols and some other novel host compounds
-
Atwood, J.L., Davies, J.E.D., MacNicol, D.D., eds. Oxford: Oxford Univ. Press
-
Toda, F. Inclusion by acetylenic alcohols and some other novel host compounds. In: Inclusion Compounds. Atwood, J.L., Davies, J.E.D., MacNicol, D.D., eds. Vol. 4, Oxford: Oxford Univ. Press, 1991:126-187.
-
(1991)
Inclusion Compounds
, vol.4
, pp. 126-187
-
-
Toda, F.1
-
11
-
-
37049090438
-
New chiral selectors derived from lactic acid. Cocrystalline and sorptive optical resolutions, and the crystal structure of an inclusion complex with 3-methyl-cyclohexanone
-
(a) Weber, E., Wimmer, C., Llamas-Saiz, A.L., Foces-Foces, C. New chiral selectors derived from lactic acid. Cocrystalline and sorptive optical resolutions, and the crystal structure of an inclusion complex with 3-methyl-cyclohexanone. J. Chem. Soc., Chem. Commun. 733-735, 1992.
-
(1992)
J. Chem. Soc., Chem. Commun.
, pp. 733-735
-
-
Weber, E.1
Wimmer, C.2
Llamas-Saiz, A.L.3
Foces-Foces, C.4
-
12
-
-
0027268631
-
Optical resolution by crystalline inclusion formation using new lactic acid derived hosts
-
(b) Weber, E., Wimmer, C. Optical resolution by crystalline inclusion formation using new lactic acid derived hosts. Chirality 5: 331-336, 1993.
-
(1993)
Chirality
, vol.5
, pp. 331-336
-
-
Weber, E.1
Wimmer, C.2
-
13
-
-
0024626258
-
Molecular recognition: Designed crystalline inclusion complexes of carboxylic hosts
-
Weber, E. Molecular recognition: Designed crystalline inclusion complexes of carboxylic hosts. J. Mol. Graphics 7:12-27, 1989.
-
(1989)
J. Mol. Graphics
, vol.7
, pp. 12-27
-
-
Weber, E.1
-
16
-
-
37049076753
-
New terpenoid hosts for chiral recognition: Crystal structure and molecular modelling study of an inclusion complex with (S)-(+)-phenyloxirane
-
Korkas, P.P., Weber, E., Czugler, M., Náray-Szabó, G. New terpenoid hosts for chiral recognition: Crystal structure and molecular modelling study of an inclusion complex with (S)-(+)-phenyloxirane, J. Chem. Soc., Chem. Commun. 2229-2230, 1995.
-
(1995)
J. Chem. Soc., Chem. Commun.
, pp. 2229-2230
-
-
Korkas, P.P.1
Weber, E.2
Czugler, M.3
Náray-Szabó, G.4
-
17
-
-
0000992810
-
New furoxan chemistry. 1. Synthesis of diarylfuroxans by reaction of ethynyl acetates with nitrosyl fluoride/nitrosium tetrafluoroborate
-
(a) Brittelli, D.R., Boswell, Jr., G.A. New furoxan chemistry. 1. Synthesis of diarylfuroxans by reaction of ethynyl acetates with nitrosyl fluoride/nitrosium tetrafluoroborate. J. Org. Chem. 46:312-315, 1981.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 312-315
-
-
Brittelli, D.R.1
Boswell Jr., G.A.2
-
18
-
-
0042406344
-
Äthinylierung bicyclischer Ketone
-
(b) Görlich, B., Hildebrandt, G. Äthinylierung bicyclischer Ketone. Chem. Ber. 91:2388-2394, 1958.
-
(1958)
Chem. Ber.
, vol.91
, pp. 2388-2394
-
-
Görlich, B.1
Hildebrandt, G.2
-
19
-
-
0004178272
-
-
Delft: Enraf-Nonius
-
CAD4 Operations Manual. Delft: Enraf-Nonius, 1977.
-
(1977)
CAD4 Operations Manual
-
-
-
20
-
-
84943920736
-
SHELXS-86. A program for the solution of crystal structures
-
Sheldrick, G.M. SHELXS-86. A program for the solution of crystal structures. Acta Crystallogr. Sect. A, 46:467-473, 1990.
-
(1990)
Acta Crystallogr. Sect. A
, vol.46
, pp. 467-473
-
-
Sheldrick, G.M.1
-
22
-
-
0342567975
-
-
This result was generated using the program Cerius 2™. This program was developed by Molecular Simulations, Inc. Burlington, MA: Molecular Simulations, Inc.
-
2 Users Guide, version 1.6, Burlington, MA: Molecular Simulations, Inc., 1994.
-
(1994)
2 Users Guide, Version 1.6
-
-
-
23
-
-
0343873727
-
-
note
-
Atomic coordinates and standard crystallographic results (bonding dimensions and Uij values) for the inclusions 1 · 3 (1:1) and 2 · 3 (1:2) have been deposited with the Cambridge Crystallographic Data Centre, Cambridge, U.K.
-
-
-
|