Enantioselective [1,2]-Stevens rearrangement of thiosulfonates to construct dithio-substituted quaternary carbon centers DOI Creative Commons
Linfeng Hu,

Jinzhao Li,

Yongyan Zhang

и другие.

Chemical Science, Год журнала: 2022, Номер 13(14), С. 4103 - 4108

Опубликована: Янв. 1, 2022

An asymmetric [1,2] Stevens rearrangement was realized via chiral guanidine and copper( i ) complexes. A series of novel dithioketal derivatives were obtained with good yields (up to 90% yield) enantioselectivities 96 : 4 er).

Язык: Английский

The chemistry and biology of guanidine secondary metabolites DOI
Roberto G. S. Berlinck, Darlon I. Bernardi, Taícia Pacheco Fill

и другие.

Natural Product Reports, Год журнала: 2020, Номер 38(3), С. 586 - 667

Опубликована: Окт. 6, 2020

Covering: 2017-2019Guanidine natural products isolated from microorganisms, marine invertebrates and terrestrial plants, amphibians spiders, represented by non-ribosomal peptides, guanidine-bearing polyketides, alkaloids, terpenoids shikimic acid derived, are the subject of this review. The topics include discovery new metabolites, total synthesis guanidine compounds, biological activity mechanism-of-action, biosynthesis ecological functions.

Язык: Английский

Процитировано

42

A Bifunctional N-Heterocyclic Carbene as a Noncovalent Organocatalyst for Enantioselective Aza-Michael Addition Reactions DOI

Fangfang Guo,

Jiean Chen, Yong Huang

и другие.

ACS Catalysis, Год журнала: 2021, Номер 11(10), С. 6316 - 6324

Опубликована: Май 11, 2021

Chiral N-heterocyclic carbenes (NHCs) have been recently established as powerful catalysts for enantioselective bond-forming processes via noncovalent interactions. The underlying HOMO-raising activation of nucleophiles takes advantage the strong Brønsted basicity NHCs. However, scope compatible electrophiles has quite limited. In this article, we report a bifunctional NHC with an embedded hydrogen-bonding motif that shows remarkable tolerance various Michael acceptors in asymmetric aza-conjugate addition reaction. catalytic efficiency far exceeds benchmark tertiary amine-thiourea scaffold.

Язык: Английский

Процитировано

37

Guanidyl-implanted UiO-66 as an efficient catalyst for the enhanced conversion of carbon dioxide into cyclic carbonates DOI

Aijia Gao,

Fangfang Li, Zhi Xu

и другие.

Dalton Transactions, Год журнала: 2022, Номер 51(6), С. 2567 - 2576

Опубликована: Янв. 1, 2022

The development of heterogeneous catalysts for promoting epoxide cycloaddition with carbon dioxide is highly desirable recycling CO2 and achieving the goal neutrality. Herein, we designed synthesized Zr-based metal organic frameworks (MOFs) by implanting functional guanidyl into framework via mixing different molar ratios 4-guanidinobenzoic acid (Gua) 1,4-benzenedicarboxylic (BDC). Consequently, a small sized Zr-MOF (∼350 nm) can be prepared Gua 20% ligands, denoted as UiO-66-Gua0.2(s). Compared to large Zr-MOFs, UiO-66-Gua0.2(s) exhibited an optimal activity on catalyzing in presence Bu4NBr cocatalyst. A yield 97% product chloropropene carbonate was achieved at 90 °C under 1 atm CO2. great performance might attributed synergistic effect groups hydrogen-bond donors Zr centers acting Lewis-acidic sites. In addition, catalyst versatility towards converting other epoxides satisfactory recyclability five consecutive runs. Moreover, plausible reaction mechanism has been proposed reactions.

Язык: Английский

Процитировано

24

Progress in (Thio)urea‐ and Squaramide‐Based Brønsted Base Catalysts with Multiple H‐Bond Donors DOI Creative Commons
Silvia Vera, Ane García‐Urricelqui, Antonia Mielgo

и другие.

European Journal of Organic Chemistry, Год журнала: 2022, Номер 26(7)

Опубликована: Дек. 15, 2022

Abstract Thiourea‐ and squaramide‐based bifunctional base catalysts represent nowadays a powerful tool in the field of asymmetric catalysis have demonstrated very efficient for promoting wide variety transformations enantioselectively. New versions that incorporate one or various additional H‐bond donor site(s) catalyst structure been developed recently which led to more active (reduced loadings) selective catalysts. This review highlights pioneering ideas most recent contributions area with material organized according nature functionality. The advantages, current limitations perspectives these new multifunctional are discussed.

Язык: Английский

Процитировано

24

Enantioselective [1,2]-Stevens rearrangement of thiosulfonates to construct dithio-substituted quaternary carbon centers DOI Creative Commons
Linfeng Hu,

Jinzhao Li,

Yongyan Zhang

и другие.

Chemical Science, Год журнала: 2022, Номер 13(14), С. 4103 - 4108

Опубликована: Янв. 1, 2022

An asymmetric [1,2] Stevens rearrangement was realized via chiral guanidine and copper( i ) complexes. A series of novel dithioketal derivatives were obtained with good yields (up to 90% yield) enantioselectivities 96 : 4 er).

Язык: Английский

Процитировано

23