Synthesis of Highly Substituted Quinolines via a Tandem Ynamide Benzannulation/Iodocyclization Strategy
A two-stage “tandem strategy” for the regiocontrolled synthesis of very highly substituted quinolines is described. Benzannulation based on the reaction of cyclobutenones or diazo ketones with N-propargyl-substituted ynamides proceeds via a cascade of several pericyclic reactions to generate multipl...
Main Authors: | Willumstad, Thomas Paul, Boudreau, Paul D, Danheiser, Rick Lane |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Chemistry |
Format: | Article |
Language: | en_US |
Published: |
American Chemical Society (ACS)
2017
|
Online Access: | http://hdl.handle.net/1721.1/108246 https://orcid.org/0000-0002-9812-206X |
Similar Items
-
Benzannulation via the Reaction of Ynamides and Vinylketenes. Application to the Synthesis of Highly Substituted Indoles
by: Lam, Tin Yiu, et al.
Published: (2014) -
Synthesis of highly substituted benzo-fused nitrogen heterocycles via tandem benzannulation/cyclization strategies
by: Willumstad, Thomas P. (Thomas Paul)
Published: (2014) -
Batch and Flow Photochemical Benzannulations Based on the Reaction of Ynamides and Diazo Ketones. Application to the Synthesis of Polycyclic Aromatic and Heteroaromatic Compounds
by: Willumstad, Thomas P., et al.
Published: (2015) -
Synthesis of Polycyclic Benzofused Nitrogen Heterocycles via a Tandem Benzannulation/Ring-Closing Metathesis Strategy. Application in a Formal Synthesis of (+)-
by: Mak, Xiao Yin, et al.
Published: (2012) -
TANDEM BENZANNULATION-CYCLIZATION STRATEGIES FOR THE SYNTHESIS OF HIGHLY SUBSTITUTED INDOLES
by: Faialaga, Nathan H.
Published: (2023)