Page 152 - Read Online
P. 152

Liu et al. Chem Synth 2023;3:22  https://dx.doi.org/10.20517/cs.2023.18          Page 9 of 9

                   enantioselective introduction of functionalized diarylmethine stereogenic centers. Angew Chem Int Ed Engl 2013;52:9229-33.  DOI
                   PubMed
               44.      Caruana L, Kniep F, Johansen TK, Poulsen PH, Jørgensen KA. A new organocatalytic concept for asymmetric α-alkylation of
                   aldehydes. J Am Chem Soc 2014;136:15929-32.  DOI  PubMed
               45.      Lou Y, Cao P, Jia T, Zhang Y, Wang M, Liao J. Copper-catalyzed enantioselective 1,6-boration of para-quinone methides and efficient
                   transformation of gem-diarylmethine boronates to triarylmethanes. Angew Chem Int Ed Engl 2015;54:12134-8.  DOI  PubMed
               46.      Wu H, Wang Q, Zhu J. Catalytic enantioselective pinacol and meinwald rearrangements for the construction of quaternary
                   stereocenters. J Am Chem Soc 2019;141:11372-7.  DOI
               47.      Lin  JS,  Li  TT,  Liu  JR,  et  al.  Cu/Chiral  phosphoric  acid-catalyzed  asymmetric  three-component  radical-initiated  1,2-
                   dicarbofunctionalization of alkenes. J Am Chem Soc 2019;141:1074-83.  DOI
               48.      Cheng Y, Fang Z, Jia Y, Lu Z, Li W, Li P. Organocatalytic enantioselective conjugate addition of 2-naphthols to ortho-hydroxyphenyl
                   substituted para-quinone methides: access to unsymmetrical triarylmethanes. RSC Adv 2019;9:24212-7.  DOI  PubMed  PMC
               49.      Zhang L, Han Y, Huang A, Zhang P, Li P, Li W. Organocatalytic remote stereocontrolled 1,8-additions of thiazolones to propargylic
                   aza-p-quinone methides. Org Lett 2019;21:7415-9.  DOI  PubMed
               50.      Li W, Xu X, Liu Y, Gao H, Cheng Y, Li P. Enantioselective organocatalytic 1,6-addition of azlactones to para-quinone methides: an
                   access to α,α-disubstituted and β, β-diaryl-α-amino acid esters. Org Lett 2018;20:1142-5.  DOI  PubMed
               51.      Wang Z, Wong YF, Sun J. Catalytic asymmetric 1,6-conjugate addition of para-quinone methides: formation of all-carbon quaternary
                   stereocenters. Angew Chem Int Ed Engl 2015;54:13711-4.  DOI  PubMed
               52.      Chen M, Sun J. How understanding the role of an additive can lead to an improved synthetic protocol without an additive:
                   organocatalytic synthesis of chiral diarylmethyl alkynes. Angew Chem Int Ed Engl 2017;56:11966-70.  DOI
               53.      Qian D, Wu L, Lin Z, Sun J. Organocatalytic synthesis of chiral tetrasubstituted allenes from racemic propargylic alcohols. Nat
                   Commun 2017;8:567.  DOI  PubMed  PMC
               54.      Ma D, Miao CB, Sun J. Catalytic enantioselective house-meinwald rearrangement: efficient construction of all-carbon quaternary
                   stereocenters. J Am Chem Soc 2019;141:13783-7.  DOI  PubMed
               55.      Li X, Duan M, Deng Z, et al. Catalytic enantioselective synthesis of chiral tetraarylmethanes. Nat Catal 2020;3:1010-9.  DOI
               56.      Li Z, Li Y, Li X, Wu M, He ML, Sun J. Organocatalytic asymmetric formal oxidative coupling for the construction of all-aryl
                   quaternary stereocenters. Chem Sci 2021;12:11793-8.  DOI  PubMed  PMC
               57.      Zhu C, Saito K, Yamanaka M, Akiyama T. Benzothiazoline: versatile hydrogen donor for organocatalytic transfer hydrogenation. Acc
                   Chem Res 2015;48:388-98.  DOI  PubMed
               58.      Osakabe H, Saito S, Miyagawa M, Suga T, Uchikura T, Akiyama T. Enantioselective dehydroxyhydrogenation of 3-indolylmethanols
                   by the combined use of benzothiazoline and chiral phosphoric acid: construction of a tertiary carbon center. Org Lett 2020;22:2225-9.
                   DOI  PubMed
               59.      Akiyama T, Itoh J, Yokota K, Fuchibe K. Enantioselective mannich-type reaction catalyzed by a chiral brønsted acid. Angew Chem Int
                   Ed Engl 2004;43:1566-8.  DOI  PubMed
               60.      Uraguchi D, Terada M. Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation. J Am Chem Soc
                   2004;126:5356-7.  DOI  PubMed
               61.      Parmar D, Sugiono E, Raja S, Rueping M. Complete field guide to asymmetric BINOL-phosphate derived Brønsted acid and metal
                   catalysis: history and classification by mode of activation; Brønsted acidity, hydrogen bonding, ion pairing, and metal phosphates.
                   Chem Rev 2014;114:9047-153.  DOI  PubMed
               62.      Akiyama T, Mori K. Stronger brønsted acids: recent progress. Chem Rev 2015;115:9277-306.  DOI  PubMed
               63.      James T, van Gemmeren M, List B. Development and applications of disulfonimides in enantioselective organocatalysis. Chem Rev
                   2015;115:9388-409.  DOI
               64.      Kikuchi J, Terada M. Enantioconvergent substitution reactions of racemic electrophiles by organocatalysis. Chemistry 2021;27:10215-
                   25.  DOI  PubMed
               65.      Han Z, Zang Y, Liu C, Guo W, Huang H, Sun J. Enantioselective synthesis of triarylmethanes via organocatalytic transfer
                   hydrogenation of para-quinone methides. Chem Commun (Camb) 2022;58:7128-31.  DOI
               66.      Wang J, Hao W, Tu S, Jiang B. Recent developments in 1,6-addition reactions of para -quinone methides (p -QMs). Org Chem Front
                   2020;7:1743-78.  DOI
   147   148   149   150   151   152   153   154   155   156   157