A Multifaceted Directing Group Switching Ynones as Michael Donors in Chemo-, Enantio-, and γ-Selective 1,4-Conjugate Additions with Nitroolefins.

α,β-Unsaturated ynones have historically been used as Michael acceptors in conjugate addition reactions. Herein, we have demonstrated for the first time that ynones can be harnessed as Michael donors for use in catalytic asymmetric conjugate addition reactions by strategically introducing a CO2t-Bu group as a multitasking directing group. Furthermore, this concept has enabled designer ynones as versatile synthetic equivalents of both α' anions of ynones and γ monoanions of 1,3-diketones, which are synthetically valued but difficult to generate. The first catalytic enantioselective conjugate addition of ynones as Michael donors has been realized in good yields with high enantioselectivities. A unified approach to regiospecifically and chemo- and enantioselectively access hitherto elusive γ-Michael adducts of 1,3-diketones has been achieved in a divergent manner. The strategy described here by exploring new reactivity and creating new reagents holds great potential applications in other still unsolved transformations.

[1]  Yujiro Hayashi,et al.  Pot economy and one-pot synthesis , 2016, Chemical science.

[2]  B. Trost,et al.  Broad Spectrum Enolate Equivalent for Catalytic Chemo-, Diastereo-, and Enantioselective Addition to N-Boc Imines. , 2015, Journal of the American Chemical Society.

[3]  Guangbin Dong,et al.  Synthesis of Ynones and Recent Application in Transition-Metal-Catalyzed Reactions , 2015 .

[4]  Z. Shao,et al.  Asymmetric synthesis of syn-propargylamines and unsaturated β-amino acids under Brønsted base catalysis , 2015, Nature Communications.

[5]  B. Hong,et al.  Asymmetric Synthesis of Natural Products and Medicinal Drugs through One-Pot-Reaction Strategies , 2015 .

[6]  Z. Shao,et al.  Catalytic asymmetric assembly of octahydroindolones: divergent synthesis of lycorine-type amaryllidaceae alkaloids (+)-α-lycorane and (+)-lycorine. , 2014, Chemistry.

[7]  Fangzhi Peng,et al.  Asymmetric catalytic conjugate addition of acetaldehyde to nitrodienynes/nitroenynes: applications to the syntheses of (+)-α-lycorane and chiral β-alkynyl acids. , 2014, Organic letters.

[8]  Magnus Rueping,et al.  Catalytic C-C bond-forming multi-component cascade or domino reactions: pushing the boundaries of complexity in asymmetric organocatalysis. , 2014, Chemical reviews.

[9]  Z. Shao,et al.  Catalytic asymmetric synthesis of 1,3-enyne scaffolds: design and synthesis of conjugated nitro dienynes as novel Michael acceptors and development of a new synthetic methodology. , 2014, Chemical communications.

[10]  B. Trost,et al.  A concise synthesis of (-)-lasonolide A. , 2014, Journal of the American Chemical Society.

[11]  Jin-liang Yang,et al.  Enantioselective [4 + 2] cycloaddition of cyclic N-sulfimines and acyclic enones or ynones: a concise route to sulfamidate-fused 2,6-disubstituted piperidin-4-ones. , 2013, Organic letters.

[12]  D. Ramachary,et al.  Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis. , 2013, Organic letters.

[13]  Z. Shao,et al.  Mutually Complementary Metal- and Organocatalysis with Collective Synthesis: Asymmetric Conjugate Addition of 1,3-Carbonyl Compounds to Nitroenynes and Further Reactions of the Products , 2012 .

[14]  M. Kanai,et al.  Copper(I)-catalyzed enantioselective incorporation of ketones to cyclic hemiaminals for the synthesis of versatile alkaloid precursors. , 2012, Journal of the American Chemical Society.

[15]  J. P. Harrity,et al.  Synthesis of ynone trifluoroborates toward functionalized pyrazoles. , 2012, Organic letters.

[16]  A. Fürstner,et al.  Total synthesis of neurymenolide A based on a gold-catalyzed synthesis of 4-hydroxy-2-pyrones. , 2012, Angewandte Chemie.

[17]  M. Kanai,et al.  Asymmetric synthesis of dihydropyranones from ynones by sequential copper(I)-catalyzed direct aldol and silver(I)-catalyzed oxy-Michael reactions. , 2012, Angewandte Chemie.

[18]  D. Ramachary,et al.  Discovery of 2-aminobuta-1,3-enynes in asymmetric organocascade catalysis: construction of drug-like spirocyclic cyclohexanes having five to six contiguous stereocenters. , 2012, Chemical communications.

[19]  K. Jørgensen,et al.  A simple recipe for sophisticated cocktails: organocatalytic one-pot reactions--concept, nomenclature, and future perspectives. , 2011, Angewandte Chemie.

[20]  B. Breit,et al.  Removable directing groups in organic synthesis and catalysis. , 2011, Angewandte Chemie.

[21]  Fangzhi Peng,et al.  Enantioselective and regioselective organocatalytic conjugate addition of malonates to nitroenynes. , 2011, Chemistry, an Asian journal.

[22]  D. Enders,et al.  Organocatalytic cascade reactions as a new tool in total synthesis. , 2010, Nature chemistry.

[23]  Z. Shao,et al.  Asymmetric Conjugate Addition of Acetylacetone to Nitroolefins with Chiral Organocatalysts Derived from Both α‐Amino ­Acids and Carbohydrates , 2009 .

[24]  A. Capretta,et al.  Access to flavones via a microwave-assisted, one-pot Sonogashira-carbonylation-annulation reaction. , 2009, Organic letters.

[25]  B. Trost,et al.  The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups. , 2009, Advanced synthesis & catalysis.

[26]  Gan-peng Li,et al.  Organocatalytic enantioselective Michael addition of 2,4-pentandione to nitroalkenes promoted by bifunctional thioureas with central and axial chiral elements. , 2008, The Journal of organic chemistry.

[27]  Y. Hayashi,et al.  Asymmetric Michael reaction of acetaldehyde catalyzed by diphenylprolinol silyl ether. , 2008, Angewandte Chemie.

[28]  B. List,et al.  Catalytic asymmetric Michael reactions of acetaldehyde. , 2008, Angewandte Chemie.

[29]  Xiaojun Wu,et al.  Chiral amine-thioureas bearing multiple hydrogen bonding donors: highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins. , 2008, Chemical communications.

[30]  S. Connon Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts. , 2008, Chemical communications.

[31]  A. Alexakis,et al.  Chiral amines as organocatalysts for asymmetric conjugate addition to nitroolefins and vinyl sulfones via enamine activation. , 2007, Chemical communications.

[32]  J. Vicario,et al.  Organocatalytic Enantioselective Michael and Hetero‐Michael Reactions , 2007 .

[33]  S. Tsogoeva Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions , 2007 .

[34]  D. Alonso,et al.  Organocatalytic asymmetric conjugate additions , 2007 .

[35]  V. Gouverneur,et al.  Enantioselective organocatalytic aldol reaction of ynones and its synthetic applications. , 2006, Organic letters.

[36]  Mark S. Taylor,et al.  Asymmetric catalysis by chiral hydrogen-bond donors. , 2006, Angewandte Chemie.

[37]  Y. Takemoto,et al.  Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors. , 2005, Organic & biomolecular chemistry.

[38]  M. Kanai,et al.  Catalyst-controlled asymmetric synthesis of fostriecin and 8-epi-fostriecin. , 2005, Journal of the American Chemical Society.

[39]  S. Connon,et al.  Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance. , 2005, Angewandte Chemie.

[40]  Jinxing Ye,et al.  Enantioselective organocatalytic Michael addition of malonate esters to nitro olefins using bifunctional cinchonine derivatives. , 2005, Chemical communications.

[41]  B. Trost,et al.  Dinuclear asymmetric Zn aldol additions: formal asymmetric synthesis of fostriecin. , 2005, Journal of the American Chemical Society.

[42]  Y. Takemoto,et al.  Enantio- and diastereoselective Michael reaction of 1,3-dicarbonyl compounds to nitroolefins catalyzed by a bifunctional thiourea. , 2005, Journal of the American Chemical Society.

[43]  L. Tang,et al.  Highly enantioselective conjugate addition of malonate and beta-ketoester to nitroalkenes: asymmetric C-C bond formation with new bifunctional organic catalysts based on cinchona alkaloids. , 2004, Journal of the American Chemical Society.

[44]  B. Trost,et al.  Direct catalytic asymmetric aldol additions of methyl ynones. Spontaneous reversal in the sense of enantioinduction. , 2004, Journal of the American Chemical Society.

[45]  S. Ley,et al.  Development of beta-keto 1,3-dithianes as versatile intermediates for organic synthesis. , 2003, Organic & biomolecular chemistry.

[46]  Alex Maioli Recent Advances in the Chemistry of 1,3-Diketones: Structural Modifications and Synthetic Applications , 2003 .

[47]  A. Kel'in Recent Advances in the Synthesis of 1,3-Diketones , 2003 .

[48]  T. Müller,et al.  New entry to a three-component pyrimidine synthesis by TMS-Ynones via Sonogashira coupling. , 2003, Organic letters.

[49]  P. Schreiner Metal-free organocatalysis through explicit hydrogen bonding interactions. , 2003, Chemical Society reviews.

[50]  Masakatsu Shibasaki,et al.  Formal catalytic asymmetric total synthesis of fostriecin. , 2003, Organic letters.

[51]  D. Enders,et al.  Asymmetric Michael Additions to Nitroalkenes , 2002 .

[52]  A. Kel'in,et al.  Efficient synthesis of 2-mono- and 2,5-disubstituted furans via the CuI-catalyzed cycloisomerization of alkynyl ketones. , 2002, The Journal of organic chemistry.

[53]  Y. Ling,et al.  Palladium-catalyzed tandem dimerization and cyclization of acetylenic ketones: a convenient method for 3,3'-bifurans using PdCl2(PPh3)2. , 2001, The Journal of organic chemistry.

[54]  N. Krause,et al.  Recent Advances in Catalytic Enantioselective Michael Additions , 2001 .

[55]  A. Kel'in,et al.  A novel Cu-assisted cycloisomerization of alkynyl imines: efficient synthesis of pyrroles and pyrrole-containing heterocycles. , 2001, Journal of the American Chemical Society.

[56]  M. Sibi,et al.  Enantioselective Conjugate Additions , 2000 .

[57]  Wang,et al.  Regioselective synthesis of unsymmetrical 3, 5-dialkyl-1-arylpyrazoles , 2000, Organic letters.

[58]  Ali,et al.  Chemo- and regioselective cyclohydrocarbonylation of alpha-keto alkynes catalyzed by a zwitterionic rhodium complex and triphenyl phosphite , 2000, The Journal of organic chemistry.

[59]  E. Rossi,et al.  Synthesis of functionalised quinolines through tandem addition/annulation reactions of β-(2-aminophenyl)-α,β-ynones , 1999 .

[60]  T. Ikariya,et al.  Asymmetric Transfer Hydrogenation of a,-Acetylenic Ketones , 1997 .

[61]  E. Corey,et al.  Direct Catalytic Enantioselective Reduction of Achiral α,β-Ynones. Strong Remote Steric Effects Across the C−C Triple Bond , 1996 .

[62]  M. Hojo,et al.  Synthesis and reactions of methyl (trimethylsilylmethyl)-acetylenecar☐ylate. A general method for the generation of di-exo-methyleneisoxazolines and novel access to fused isoxazoles , 1993 .

[63]  H. Miwa,et al.  Palladium-catalyzed synthesis of pyrroles , 1982 .

[64]  D. Seebach,et al.  Addition of Oxoalkane Polyanions to Nitroolefins. A New Synthesis of Cyclohexanones , 1974 .