Synthesis of cis-Fused Carbo-Bicycles by Domino Enyne Cross-Metathesis/Intramolecular Diels−Alder Reaction
Author:
Affiliation:
1. Institut für Chemie, Technische Universität Berlin, Strasse des 17. Juni 135, 10623 Berlin, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol050508c
Reference17 articles.
1. A Crossed Yne–Ene Metathesis Showing Atom Economy
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3. Enyne Metathesis (Enyne Bond Reorganization)
4. A Series of Well-Defined Metathesis Catalysts–Synthesis of[RuCl2(CHR′)(PR3)2] and Its Reactions
5. Synthesis and Activity of a New Generation of Ruthenium-Based Olefin Metathesis Catalysts Coordinated with 1,3-Dimesityl-4,5-dihydroimidazol-2-ylidene Ligands
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1. Original Mitsunobu-Triggered Sequence Involved in a One-Pot Domino Process toward Tetracyclic Systems Bearing a Bis-N,O-acetal Junction;The Journal of Organic Chemistry;2016-09-16
2. Tandem cross enyne metathesis (CEYM)–intramolecular Diels–Alder reaction (IMDAR). An easy entry to linear bicyclic scaffolds;Beilstein Journal of Organic Chemistry;2015-08-25
3. Access to Functionalized α-Trifluoromethyl-α-aminophosphonates via Intermolecular Ene–Yne Metathesis;Synlett;2014-10-15
4. Ring-Closing Metathesis Reactions of Bis(enynes): Selectivity and Surprises;The Journal of Organic Chemistry;2014-06-03
5. Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds;Tetrahedron;2014-05
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