We describe a photoinduced copper‐catalyzed asymmetric radical decarboxylative alkynylation of bench‐stable N‐hydroxyphthalimide(NHP)‐type esters of racemic alkyl carboxylic acids with terminal alkynes, which provides a flexible platform for the construction of chiral C(sp3)−C(sp) bonds. Critical to the success of this process are not only the use of the copper catalyst as a dual photo‐ and cross‐coupling catalyst but also tuning of the NHP‐type esters to inhibit the facile homodimerization of the alkyl radical and terminal alkyne, respectively. Owing to the use of stable and easily available NHP‐type esters, the reaction features a broader substrate scope compared with reactions using the alkyl halide counterparts, covering (hetero)benzyl‐, allyl‐, and aminocarbonyl‐substituted carboxylic acid derivatives, and (hetero)aryl and alkyl as well as silyl alkynes, thus providing a vital complementary approach to the previously reported method.
The ring-opening polymerization (ROP) of trimethylene carbonate (TMC) using imidodiphosphoric acid (IDPA) as the organocatalyst and benzyl alcohol (BnOH) as the initiator has been investigated. The polymerization proceeded without decarboxylation to afford poly(trimethylene carbonate) (PTMiC) with controlled molecular weight and narrow polydispersity. 1 H NMR, SEC, and MALDI-TOF MS measurements of the obtained PTMC clearly indicated the quantitative incorporation of the initiator at the chain end. The controlled/living nature for the IDPA-catalyzed ROP of TMC was confirmed by the kinetic and chain extension experiments. A bifunctional activation mechanism was proposed for IDPA catalysis based on NMR and FTIR studies. Additionally, 1,3-propanediol, 1,1,1-trimethy-lolpropane, and pentaerythritol were used as di-ol, tri-, and tetra-ol initiators, producing the telechelic or star-shaped polycarbonates with narrow polydispersity indices. The welldefined diblock copolymers, poly(trimethylene carbonate)block-poly(d-valerolactone) and poly(trimethylene carbonate)block-poly(e-caprolactone), have been successfully synthesized by using the IDPA catalysis system.
An organocatalytic approach to controlled/living ring-opening polymerizations (ROPs) of O-carboxyanhydrides (OCAs) using N-heterocyclic carbenes (NHCs) as nucleophilic catalysts has been investigated. NHCs with different structures were used in order to compare the catalytic performances in the ROP of OCA of L-lactic acid.1 H NMR, SEC, and MALDI-TOF MS measurements of the products clearly indicated a controlled/living manner of the polymerization. The controlled/living nature was further confirmed by kinetic and chain extension experiments. Additionally, polylol initiators were used to produce a,x-dihydroxy telechelic, 3-, and 4-armed starshaped polymers. Moreover, star-shaped diblock copolymer, bearing methyl and phenyl side groups, has been successfully synthesized with OCA/NHC system.
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