Trithioorthoester Exchange and Metathesis: New Tools for Dynamic Covalent Chemistry

Synlett ◽  
2019 ◽  
Vol 30 (17) ◽  
pp. 1988-1994
Author(s):  
Michael Bothe ◽  
A. Gastón Orrillo ◽  
Ricardo L. E. Furlan ◽  
Max von Delius

To expand the toolbox of dynamic covalent and systems chemistry, we investigated the acid-catalyzed exchange reaction of trithioorthoesters with thiols. We found that trithioorthoester exchange occurs readily in various solvents in the presence of stoichiometric amounts of strong Brønsted acids or catalytic amounts of certain Lewis acids. The scope of the exchange reaction was explored with various substrates, and conditions were identified that permit clean metathesis reactions between two different trithioorthoesters. One distinct advantage of S,S,S-orthoester exchange over O,O,O-orthoester exchange is that the exchange reaction can kinetically outcompete hydrolysis, thereby making the process less sensitive to residual moisture. We expect that the relatively high stability of the products might be beneficial in future supramolecular receptors or porous materials.

Synthesis ◽  
2021 ◽  
Author(s):  
Heather Lam ◽  
Mark Lautens ◽  
Xavier Abel-Snape ◽  
Martin F. Köllen

Abstract(4+3)-Annulations are incredibly versatile reactions which combine a 4-atom synthon and a 3-atom synthon to form both 7-membered carbocycles as well as heterocycles. We have previously reviewed transition-metal-catalyzed (4+3)-annulations. In this review, we will cover examples involving bases, NHCs, phosphines, Lewis and Brønsted acids as well as some rare examples of boronic acid catalysis and photocatalysis. In analogy to our previous review, we exclude annulations involving cyclic dienes like furan, pyrrole, cyclohexadiene or cyclopentadiene, as Chiu, Harmata, Fernándes and others have recently published reviews encompassing such substrates. We will however discuss the recent additions (2010–2020) to the literature on (4+3)-annulations involving other types of 4-atom-synthons.1 Introduction2 Bases3 Annulations Using N-Heterocyclic Carbenes3.1 N-Heterocyclic Carbenes (NHCs)3.2 N-Heterocyclic Carbenes and Base Dual-Activation4 Phosphines5 Acids5.1 Lewis Acids5.2 Brønsted Acids6 Boronic Acid Catalysis and Photocatalysis7 Conclusion


2009 ◽  
Vol 11 (6) ◽  
pp. 1313-1316 ◽  
Author(s):  
Nobuhiro Kihara ◽  
Kazuyuki Kidoba

ChemInform ◽  
2006 ◽  
Vol 37 (31) ◽  
Author(s):  
Martin A. Iglesias-Arteaga ◽  
Izabella Jastrzebska ◽  
Jacek W. Morzycki
Keyword(s):  

1979 ◽  
Vol 57 (22) ◽  
pp. 2896-2901 ◽  
Author(s):  
Robert A. McClelland ◽  
William F. Reynolds

Rate constants have been obtained for the acid-catalyzed N–H exchange of N-methyl, 2,N-dimethyl, and 2,4,6,N-tetramethylbenzamide and the acid-catalyzed isomerization of the three corresponding N,N-dimethylbenzamides. The ratio [Formula: see text] increases significantly with increased number of ortho methyl substituents. This is explained in terms of a suggestion of Perrin, that C—N bond rotation is not completely free in the N-protonated amide, since it must compete with a diffusion limited deprotonation reaction. The isomerization reaction, which requires such a rotation, is therefore slowed by ortho methyl substituents which hinder rotation, relative to the exchange reaction, which does not require rotation.


2017 ◽  
Vol 8 (10) ◽  
pp. 7197-7202 ◽  
Author(s):  
Guo-Peng Wang ◽  
Meng-Qing Chen ◽  
Shou-Fei Zhu ◽  
Qi-Lin Zhou

The first enantioselective Nazarov cyclization of substrates with only one coordinating site and with proton-transfer as an enantioselective-determining step was realized by means of cooperative catalysis with a Lewis acid and a chiral Brønsted acid.


RSC Advances ◽  
2016 ◽  
Vol 6 (31) ◽  
pp. 25703-25712 ◽  
Author(s):  
Naganna Narra ◽  
Badari Narayana Prasad Rachapudi ◽  
Sahithya Phani Babu Vemulapalli ◽  
Padmaja V. Korlipara

Novel bio-based cyclic carbonates were synthesised from ricinoleic acid by intra molecular rearrangement of an epoxy carbonate ester with Lewis acids.


Sign in / Sign up

Export Citation Format

Share Document