Abstract
The preparations and structures of LAlOCH2C(S)HMeCl, where L = (R,R) or (S,S)-N,N′-bis(3,5-di-tert-butyl-salicylidene)-1,2- cyclohexenediamino, are reported together with the respective LAlOEt compounds, and their reactivities toward L- and rac-lactides in various solvents reveal the surprising complexity of the stereopreference for the ring-opening event.
| Original language | English |
|---|---|
| Pages (from-to) | 127-129 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Issue number | 1 |
| Early online date | 25 Nov 2004 |
| DOIs | |
| Publication status | Published - 7 Jan 2005 |
| Externally published | Yes |
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Dive into the research topics of 'Concerning the relative importance of enantiomorphic site vs. chain end control in the stereoselective polymerization of lactides: Reactions of (R,R-salen)- and (S,S-salen)-aluminium alkoxides LAlOCH2R complexes (R = CH3 and S-CHMeCl)'. Together they form a unique fingerprint.Cite this
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