Synthesis of substituted γ- and δ-lactams through mannich-type reactions of solid-supported N -acyliminium ions
We report the results of our recent investigations into the reactivity of cyclic solid-supported N-acyliminium ions. An intermolecular Mannich-type transformation of these intermediates was used to generate libraries of substituted lactams. Masked aldehyde building blocks were readily prepared and c...
Main Authors: | Komnatnyy, Vitaly V., Taveras, Kennedy M., Nandurkar, Nitin S., Le Quement, Sebastian T., Givskov, Michael, Nielsen, Thomas Eiland |
---|---|
Other Authors: | Singapore Centre for Environmental Life Sciences Engineering |
Format: | Journal Article |
Language: | English |
Published: |
2015
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/107485 http://hdl.handle.net/10220/25576 http://dx.doi.org/10.1002/ejoc.201500054 |
Similar Items
-
Solid-phase synthesis of structurally diverse heterocycles by an amide-ketone condensation/N-acyliminium Pictet-Spengler sequence
by: Givskov, Michael, et al.
Published: (2013) -
Reductive cyclization and petasis-like reaction for the synthesis of functionalized γ-lactams
by: Wu, Peng, et al.
Published: (2015) -
The development of nitro-Mannich/hydroamination cascades for the synthesis of substituted N-heterocycles
by: Barber, D, et al.
Published: (2013) -
Organic Brønsted acid-catalysed enantioselective N-acyliminium cyclisation cascades
by: Muratore, M, et al.
Published: (2010) -
Preparation and some reactions of an α-lactam
by: Lengyel, István.
Published: (2022)