Chirality-directed organogel formation
New low molecular mass enantiopure organogelators (1 R,4 R)- 1, ( S)- 2, ( R)- 3 and ( R)- 4 were found; racemates ( R,S)- 3 and ( R,S)- 4 have only a moderate gelating power, whereas ( R,S)- 1 and ( R,S)- 2 do not show gelating properties at all.
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Veröffentlicht in: | Mendeleev communications 2005, Vol.15 (4), p.140-141 |
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container_issue | 4 |
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container_title | Mendeleev communications |
container_volume | 15 |
creator | Kostyanovsky, Remir G. Lenev, Denis A. Krutius, Oleg N. Stankevich, Andrey A. |
description | New low molecular mass enantiopure organogelators (1
R,4
R)-
1, (
S)-
2, (
R)-
3 and (
R)-
4 were found; racemates (
R,S)-
3 and (
R,S)-
4 have only a moderate gelating power, whereas (
R,S)-
1 and (
R,S)-
2 do not show gelating properties at all. |
doi_str_mv | 10.1070/MC2005v015n04ABEH002136 |
format | Article |
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R)-
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R,4
R)-
1, (
S)-
2, (
R)-
3 and (
R)-
4 were found; racemates (
R,S)-
3 and (
R,S)-
4 have only a moderate gelating power, whereas (
R,S)-
1 and (
R,S)-
2 do not show gelating properties at all.</abstract><pub>Elsevier B.V</pub><doi>10.1070/MC2005v015n04ABEH002136</doi><tpages>2</tpages></addata></record> |
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issn | 0959-9436 |
language | eng |
recordid | cdi_crossref_primary_10_1070_MC2005v015n04ABEH002136 |
source | ScienceDirect Journals (5 years ago - present) |
title | Chirality-directed organogel formation |
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