Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/82223
Title: | Carbene-catalyzed desymmetrization of 1,3-diols: access to optically enriched tertiary alkyl chlorides | Authors: | Li, Bao-Sheng Wang, Yuhuang Proctor, Rupert S. J. Jin, Zhichao Chi, Yonggui Robin |
Keywords: | Tertiary alkyl chlorides Carbene-catalyzed reactions |
Issue Date: | 2016 | Source: | Li, B.-S., Wang, Y., Proctor, R. S. J., Jin, Z., & Chi, Y. R. (2016). Carbene-catalyzed desymmetrization of 1,3-diols: access to optically enriched tertiary alkyl chlorides. Chemical Communications, 52(53), 8313-8316. | Series/Report no.: | Chemical Communications | Abstract: | The introduction of a chlorine atom to a carbon center in an enantioselective manner via conventional C–Cl bond formation is difficult. Here we report a new approach to this class of tertiary alkyl chlorides with high optical purities. Instead of forming a new C–Cl bond, our approach involves carbene-catalyzed desymmetrization of 2-chloro-1,3-diols as the key step to set up the chiral carbon center with excellent enantiomeric excess. | URI: | https://hdl.handle.net/10356/82223 http://hdl.handle.net/10220/43497 |
ISSN: | 1359-7345 | DOI: | 10.1039/C6CC03345H | Rights: | © 2016 The Royal Society of Chemistry. This is the author created version of a work that has been peer reviewed and accepted for publication by Chemical Communications, The Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/C6CC03345H]. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SPMS Journal Articles |
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Carbene-catalyzed desymmetrization of 1,3-diols _ access to optically enriched tertiary alkyl chlorides.pdf | 1.16 MB | Adobe PDF | ![]() View/Open |
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