Regioselective trans-Carboboration of Propargyl Alcohols
Author:
Affiliation:
1. Max-Planck-Institut für Kohlenforschung, 45470 Mülheim/Ruhr, Germany
Funder
Max-Planck-Gesellschaft
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b01225
Reference44 articles.
1. trans-Hydrogenation, gem-Hydrogenation, and trans-Hydrometalation of Alkynes: An Interim Report on an Unorthodox Reactivity Paradigm
2. Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes
3. Selective Formation of a Trisubstituted Alkene Motif bytrans-Hydrostannation/Stille Coupling: Application to the Total Synthesis and Late-Stage Modification of 5,6-Dihydrocineromycin B
4. A “Motif-Oriented” Total Synthesis of Nannocystin Ax. Preparation and Biological Assessment of Analogues
5. Total Synthesis of Disciformycin A and B: Unusually Exigent Targets of Biological Significance
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