Highly Active Chiral Ruthenium Catalysts for Asymmetric Cross- and Ring-Opening Cross-Metathesis.

ChemInform ◽  
2007 ◽  
Vol 38 (12) ◽  
Author(s):  
Jacob M. Berlin ◽  
Steven D. Goldberg ◽  
Robert H. Grubbs
2006 ◽  
Vol 118 (45) ◽  
pp. 7753-7757 ◽  
Author(s):  
Jacob M. Berlin ◽  
Steven D. Goldberg ◽  
Robert H. Grubbs

2006 ◽  
Vol 45 (45) ◽  
pp. 7591-7595 ◽  
Author(s):  
Jacob M. Berlin ◽  
Steven D. Goldberg ◽  
Robert H. Grubbs

Synfacts ◽  
2007 ◽  
Vol 2007 (2) ◽  
pp. 0185-0185 ◽  
Author(s):  
R. Grubbs ◽  
J. Berlin ◽  
S. Goldberg

2018 ◽  
Author(s):  
Nicholas Marshall

A set of experiments in surface-initiated ring-opening metathesis polymerization, including end-functionalization of growing brushes and contact angle/cyclic voltammetry measurements. We report preparation and CV of two different conjugated polymer films, and several endgroup and sidechain functionalization experiments using cross-metathesis and active ester substitution.<br>


2021 ◽  
Vol 12 (13) ◽  
pp. 1957-1966
Author(s):  
Xinya Wang ◽  
Xiaohua Wang ◽  
Nuo Zhen ◽  
Jin Gu ◽  
Hao Zhang ◽  
...  

Sodium complexes displaying cavity-like conformations and, therefore, suppressed transesterification during the ring-opening polymerization of pentadecalactone are disclosed herein.


Synlett ◽  
2021 ◽  
Author(s):  
Loránd Kiss ◽  
Zsanett Benke ◽  
Melinda Nonn ◽  
Attila M. Remete ◽  
Santos Fustero

AbstractThis Account gives an insight into the selective functionalization of some readily available commercial cyclodienes across simple chemical transformations into functionalized small-molecular scaffolds. The syntheses involved selective cycloadditions, followed by ring-opening metathesis (ROM) of the resulting azetidin-2-one derivatives or isoxazoline frameworks and selective cross metathesis (CM) by discrimination of the C=C bonds on the alkenylated heterocycles. The CM protocols have been described when investigated under various conditions with the purpose on exploring chemodifferentiation of the olefin bonds and a study on the access of the corresponding functionalized β-lactam or isoxazoline derivatives is presented. Due to the expanding importance of organofluorine chemistry in drug research as well as of the high biological potential of β-lactam derivatives several illustrative examples to the access of some fluorine-containing molecular entities is also presented in this synopsis.1 Introduction2 Ring C=C Bond Functionalization of Some Cycloalkene β-Amino Acid Derivatives across Chlorosulfonyl Isocyanate Cycloaddition3 Ring C=C Bond Functionalization of Some Cycloalkene β-Amino Acid Derivatives across Nitrile Oxide Cycloaddition4 Ring C=C Bond Functionalization of Some Cycloalkene β-Amino Acid Derivatives across Metathesis5 Functionalization of sSome Cyclodienes across Nitrile Oxide Cycloaddition6 Selective Synthesis of Functionalized Alicycles across Ring-Opening Metathesis7 Selective Synthesis of Functionalized Alicycles through Cross Metathesis8 Summary and Outlook9 List of Abbreviations


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