731 to 740 of 764 Results
Jan 19, 2022 -
A Triptycene-Based Enantiopure Bis(Diazadibenzoanthracene) by a Chirality-Assisted Synthesis Approach [Data]
ZIP Archive - 94.0 MB -
MD5: 428a5453cd7bb2cbf52e94a462992e27
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Jan 19, 2022 -
A Triptycene-Based Enantiopure Bis(Diazadibenzoanthracene) by a Chirality-Assisted Synthesis Approach [Data]
ZIP Archive - 109.2 MB -
MD5: bbf15c5340dce284f5ec142171c7f852
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Jan 19, 2022 -
A Triptycene-Based Enantiopure Bis(Diazadibenzoanthracene) by a Chirality-Assisted Synthesis Approach [Data]
ZIP Archive - 75.1 MB -
MD5: cda821ac0af96e656f76a211dca51fec
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Jan 17, 2022 - Institute of Organic Chemistry - AK Mastalerz
Holsten, Mattes; Feierabend, Sarah; Elbert, Sven M.; Rominger, Frank; Oeser, Thomas; Mastalerz, Michael, 2022, "Soluble Congeners of Prior Insoluble Shape‐Persistent Imine Cages [Data]", https://doi.org/10.11588/data/E2RPGA, heiDATA, V1
One of the most applied reaction types to synthesize shape‐persistent organic cage compounds is the imine condensation reaction and it is assumed that the formed cages are thermodynamically controlled products due to the reversibility of the imine condensation. However, most of t... |
ZIP Archive - 109.3 MB -
MD5: ce1d3715c87cbe5c42890301218ee9a3
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ZIP Archive - 104.6 MB -
MD5: 9c81219a9c839f4bb5efded1b0841759
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ZIP Archive - 106.8 MB -
MD5: f4953cfa1d52cf5bf8edd5c0a31b34ac
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ZIP Archive - 102.9 MB -
MD5: a4640c826c195273c2a9a71bd9da0d04
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ZIP Archive - 47.7 MB -
MD5: 0bcff31f1c072b7d61f276cc2d3939bf
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ZIP Archive - 107.7 MB -
MD5: ab691d40bfb20f57b0e9e903d340a4a9
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