English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Total Synthesis of Tulearin C

MPS-Authors
/persons/resource/persons58745

Lehr,  Konrad
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58798

Mariz,  Ronaldo
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58752

Leseurre,  Lucie
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58558

Gabor,  Barbara
Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

/persons/resource/persons58380

Fürstner,  Alois
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

Locator
There are no locators available
Fulltext (public)
There are no public fulltexts available
Supplementary Material (public)

anie_201106117_sm_miscellaneous_information.pdf
(Supplementary material), 7MB

Citation

Lehr, K., Mariz, R., Leseurre, L., Gabor, B., & Fürstner, A. (2011). Total Synthesis of Tulearin C. Angewandte Chemie International Edition, 50(48), 11373-11377. doi:10.1002/anie.201106117.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0014-CA21-7
Abstract
With the help of the smaller brother: Although alkyne metathesis will always be the little brother of alkene metathesis, it allows problems to be solved that are currently beyond reach of the more famous sibling. This notion is exemplified by the tulearin macrolides, which could only be selectively forged by ring-closing alkyne metathesis (RCAM)/trans reduction using the latest generation of alkyne metathesis catalysts.