scholarly journals Book Reviews

2013 ◽  
Vol 34 (3) ◽  
Author(s):  
Joann Kovacich

Annual Review of Gerontology and Geriatrics 2010-2013 Volume 30, 2010: Focus on Biobehavioral Perspectives on Health in Late Life (Keith E. Whitfield, ed.) Linda J. Keilman , Michigan State University Volume 31, 2011: Pathways Through the Transitions of Care for Older Adults. (Peggye Dilworth-Anderson and Mary H. Palmer, eds.) Rachel Sona Reed, The Pasadena Village Volume 32, 2012: Emerging Perspectives on Resilience in Adulthood and Later Life (Bert Hayslip Jr., Gregory Smith, eds.) Lydia K. Manning, Concordia University, Chicago Volume 33, 2013. Healthy Longevity: A Global Approach (Jean-Marie Robine, Carol Jagger, and Eileen M. Crimmins, eds.) Richard Zimmer, Sonoma State UniversityTranscending Dementia through the TTAP Method:  A New Psychology of Art, Brain, and Cognition (Linda Levine Madori) Jennifer A. Wagner, Bowling Green UniversityHandbook of Life-Span Development (Karen L. Fingerman, Cynthia A. Berg, Jacqui Smith & Toni C. Antonucci, eds.) Ruth N. Grendell, University of Phoenix/Point Loma Nazarene UniversityHealth, Illness, and Optimal Aging: Biological and Psychosocial Perspectives Second Edition. (Caolyn M. Aldwin and Diane Gilmer Fox) Elisha R. Oliver, University of OklahomaBy Himself: The Older Man’s Experience of Widowhood. (Deborah K. Van den Hoonaard) Lindsay L. Martin, Michael E. DeBakey VA Medical CenterThe Validation Breakthrough: Simple Techniques for Communicating with People with Alzheimer’s and Other Dementias. Third Edition (Naomi Feil and Vicki de Klerk-Rubin) Stacey L. Barnes, Marquette UniversityGrandma, a Thousand Times (Teta, Alf Marra) (Film) Philip Kao, University of Pittsburgh

2021 ◽  
Vol 59 (1) ◽  
pp. 291-294

John D. Wilson of Michigan State University reviews “Democratic Federalism: The Economics, Politics, and Law of Federal Governance” by Robert P. Inman and Daniel L. Rubinfeld. The Econlit abstract of this book begins: “Analyzes the contemporary arguments for the democratic federal state, investigating how best to design the institutions of federal governance to achieve economic efficiency, democratic participation, and the protection of individual rights and liberties.”


Author(s):  
Douglass F. Taber

Martin Oestreich of the Technische Universität Berlin developed (Eur. J. Org. Chem. 2014, 2077) the Birch reduction product 2 as a donor for the silylation of an alco­hol 1 to give 3. Atahualpa Pinto of the SUNY College of Environmental Science and Forestry devised (Tetrahedron Lett. 2014, 55, 2600) conditions for the monosilylation of the diol 4 to give 5. Quanxuan Zhang of Michigan State University reported (Tetrahedron Lett. 2014, 55, 3384) the preparation (not illustrated) of the mono-THP ethers of symmetrical diols. The product from the Mitsunobu cou­pling of an acid with an alcohol 6 can be difficult to purify. Takashi Sugimura of the University of Hyogo showed (Synthesis 2013, 45, 931) that the oxidation product from 7 and the reduction product from 8 could both be removed from the product 9 by simple extraction. David Milstein of the Weizmann Institute of Science found (Angew. Chem. Int. Ed. 2014, 53, 4685) that an Fe catalyst could be used to reduce the trifluoroacetate 10 to 11. Jean-Michel Vatèle of the Université Lyon 1 oxidized (Synlett 2014, 25, 115) the benzylidene acetal 12 selectively to the monobenzoate 13. Xinyu Liu of the University of Pittsburgh organized (Chem. Commun. 2014, 50, 3155) a family of acid-sensitive esters that can be selectively removed in the presence of other esters, as exemplified by the conversion of 14 to 15. Ryo Yazaki and Takashi Ohshima of Kyushu University observed (Angew. Chem. Int. Ed. 2014, 53, 1611) that an amine would add spontaneously to acrylonitrile 17 to give 18. In the presence of a Cu catalyst, alcohols added to 17 even more readily, allowing the preparation of 18 from 16. Diego Gamba-Sánchez of the Universidad de los Andes used (J. Org. Chem. 2014, 79, 4544) simple Fe catalysts to activate a wide range of amides, including 20, to become acylating agents, converting 19 to 21. 1,2-Addition to t-butylsulfanylimines is widely used to construct aminated stereo­genic centers. Xiaodong Yang and Hongbin Zhang of Yunnan University established (Chem. Commun. 2014, 50, 6259) a general protocol for cleaving the N–S bond in the product 22 to give the desired free amine 23.


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