{"product_id":"organic-syntheses-volume-91-isbn-9781119054160","title":"Organic Syntheses, Volume 91","description":"\u003cp\u003eThe demand for synthetic procedures that can be duplicated may be less egregious today than in 1921, but there is still a need. To date, \u003ci\u003e\u003cb\u003eOrganic Syntheses\u003c\/b\u003e\u003c\/i\u003e has filled this need with 90 volumes of \"checked\" experimentals; and with the culmination of Kay Brummond's term as a member of the editorial board, the addition of \u003cb\u003eVolume 91\u003c\/b\u003e.\u003c\/p\u003e Discussion Addendum: Resolution of 1,1'-Bi-2-Naphthol; (R)-(+)- and (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl(BINAP) 1\u003cbr\u003e\u003ci\u003eDavid L. Hughes\u003c\/i\u003e \u003cp\u003eDiscussion Addendum for: Practical Synthesis of Novel Chiral Allenamides: (R)-4-Phenyl-3-(1,2-propadienyl)oxazoldin-2-one 12\u003cbr\u003e\u003ci\u003eYong-Chua Teo and Richard P. Hsung\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eN-Carboxylated-2-substituted Indoles and 2,3-Disubstituted-2,3-dihydro-4-quinolones from 2-Alkynylbenzamides 27\u003cbr\u003e\u003ci\u003eNoriko Okamoto, Kei Takeda, and Reiko Yanada\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003ePd-Catalyzed External-CO-Free Carbonylation: Preparation of 2,4,6-Trichlorophenyl 3,4-Dihydronaphthalene-2-Carboxylate 39\u003cbr\u003e\u003ci\u003eHideyuki Konishi, Tsuyoshi Ueda, and Kei Manabe\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eRhodium-Catalyzed Direct Amination of Arene C-H Bonds Using Azides as the Nitrogen Source 52\u003cbr\u003e\u003ci\u003eSae Hume Park, Yoosu Park, and Sukbok Chang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of Alkynyliodonium Salts: Preparation of Phenyl (phenylethynyl)iodonium Trifluoroacetate 60\u003cbr\u003e\u003ci\u003eLuke I. Dixon, Michael A. Carroll, George J. Ellames and Thomas J. Gregson\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003ePalladium-catalyzed 1,4-Addition of Terminal Alkynes to Conjugated Enones 72\u003cbr\u003e\u003ci\u003eFeng Zhou, Liang Chen and Chao-Jun Li\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eCross-Coupling of Alkenyl\/Aryl Carboxylates with Grignard Reagents via Fe-Catalyzed C-O Bond Activation 83\u003cbr\u003e\u003ci\u003eBi-Jie Li, Xi-Sha Zhang and Zhang-Jie Shi\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003ePreparation of 5-Hydroxycyclopentenones Via Conjugate Addition-Initiated Nazarov Cyclization 93\u003cbr\u003e\u003ci\u003eJoshua L. Brooks, Yu-Wen Huang, and Alison J. Frontier\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of Arylboronic Pinacol Esters from Corresponding Arylamines 106\u003cbr\u003e\u003ci\u003eDi Qiu, He Meng, Liang Jin, Shengbo Tang, Shuai Wang, Fangyang Mo, Yan Zhang and Jianbo Wang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003ePreparation of Alkanesulfonyl Chlorides from S-Alkyl Isotghiourea Salts via N-Chlorosuccinimide Mediated Oxidative Chlorosulfonation 116\u003cbr\u003e\u003ci\u003eZhanhui Yang and Jiaxi Xu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eDABCO-bis(sulfur dioxide), DABSO, as an easy-to-handle source of SO2: Sulfonamide preparation 125\u003cbr\u003e\u003ci\u003eEdward J. Emmett and Michael C. Willis\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eOne-pot Preparation of (S)-N-[(S)-1-Hydroxy-4-metghyl-1,1-diphenylpentan-2-yl]pyrrolidine-2-carboxamide from L-Proline 137\u003cbr\u003e\u003ci\u003eWacharee Hamying, Nonognaphat Duangdee, and Albrecht Berkessel\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eEnantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use of Taddol-pyrrolidine Phosphoramidite 150\u003cbr\u003e\u003ci\u003eKevin M. Oberg, Timothy J. Martin, Mark Emil Oinen, Derek M. Dalton, Rebecca Keller Friedman, Jamie M. Neely, and Tomislav Rovis\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis and Use of a Trifluoromethylated Azomethine Ylide Precursor: Ethyl 1-Benzyl-trans-5-(trifluoromethyl)pyrrolidine-3-carboxylate 162\u003cbr\u003e\u003ci\u003eDaniel M. Allwood, Duncan L. Browne and Steven V. Ley\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eEnantioselective Organocatalytic-α-Arylation of Aldehydes 175\u003cbr\u003e\u003ci\u003ePernille H. Poulsen, Mette Overgaard, Kim L. Jensen and Kari Anker Jørgensen\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of 4,5-Disubstituted 2-aminothiazoles from α,β-Unsaturated Ketones: Preparation of S-benzyl-4-methyl-2-aminothiazolium Hydrochloride salt 185\u003cbr\u003e\u003ci\u003eAntonio Bermejo Gómez, Nanna Ahlsten, Ana E. Platero-Prats and Belen Martin-Matute\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSodium Methoxide-Catalyzed Direct Amidation of Esters 201\u003cbr\u003e\u003ci\u003eKazushi Agura, Takashi Ohshima, Yukiko Hayashi, And Kazushi Mashima\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of Tetrasubstituted 1H-Pyrazoles by Copper-mediated Coupling of Enaminones with Nitriles 211\u003cbr\u003e\u003ci\u003eMamta Suri and Frank Glorius\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of 1,3-Dimethyl-3-(p-tolyl)-1H-pyrrolo[3,2-c]pyridin-2(3H)-one by Cu(II)-Mediated Direct Oxidative Coupling 221\u003cbr\u003e\u003ci\u003eChandan Dey and E. Peter Kundig\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003ePreparation of (R)-4-Cyclohexyl-2,3-butadien-1-ol 233\u003cbr\u003e\u003ci\u003eJuntao Ye and Shengming\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eDiscussion Addendum for: Formation of y-Keto Esters from β-Keto Esters: Methyl 5,5-dimethyl-4-oxohexanoate 248\u003cbr\u003e\u003ci\u003eYashoda M. D. Bhogadhi and Charles K. Zercher\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eNi-catalyzed Reductive Cleavage of Methyl 3-Methoxy-2-Naphthoate 260\u003cbr\u003e\u003ci\u003eJosep Cornella, Cayetana Zarate, and Ruben Martin\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eIndium-Catalyzed Heteroaryl-Heteroaryl Bond Formation through Nucleophilic Aromatic Substitution: Preparation of 2-Methyl-3-(thien-2-yl)-1H-indole 273\u003cbr\u003e\u003ci\u003eYuta Nagase and Teruhisa Tsuchimoto\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eSynthesis of 2,3-Disubstituted Benzofurans by the Palladium-Catalyzed Coupling of 2-Iodoanisoles and Terminal Alkynes, Followed by Electrophilic Cyclization: 3-Iodo-2-phenylbenzofuran 283\u003cbr\u003e\u003ci\u003eTuanli Yao, Dawei Yue, and Richard C. Larock\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eEnantioselective Preparation of (S)-5-Oxo-5,6-dihydro-2H-oyran-2-yl Benzoate 293\u003cbr\u003e\u003ci\u003eTamas Benkovics, Adrian Ortiz, Zhiwei Guo, Animesh Goswami and Prashant Deshpande\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eIron-Catalyzed Selective Conjugate Addition of Aryl Grignard Reagents to 2,4-Alkadienoates: tert-Butyl (Z)-5-Phenyl-3-hexenoate 307\u003cbr\u003e\u003ci\u003eTakeshi Hata, Hideyuki Goto, Tomofumi Yokomizo, and Hirokazu Urabe\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e3-Hydrixymethyl-3-phenylcyclopropene 322\u003cbr\u003e\u003ci\u003eRamajeyam Selvaraj, Srinvasa R. Chintala, Michael T. Taylor and Joseph M. Fox\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eEnantioselective Synthesis of α- and β-Boc-protected 6-Hydroxy-pyranones: Carbohydrate Building Blocks 338\u003cbr\u003e\u003ci\u003eSumit O. Bajaj, Jamison R. Farnsworth and George A. O'Doherty  \u003c\/i\u003e\u003c\/p\u003e  \u003cp\u003e\u003cstrong\u003eKay M. Brummond\u003c\/strong\u003e, Ph.D., is a researcher in the field synthetic organic chemistry. She has published 50 journal articles, 15 reviews and book chapters and delivered over 140 invited lectures and symposia. The students and postdoctoral fellows in her group have presented 52 conference posters and presentations. Nineteen graduate students have obtained Ph.D. and M.S. degrees under her direction. She is a recipient of the Chancellor's Distinguished Research Award from the University of Pittsburgh, the 2006 ACS Akron Section Award, the Carnegie Science Center Emerging Female Scientist Award and the Johnson \u0026amp; Johnson Focused Giving Award. She is on the Board of Editors of \u003cem\u003eExcellence for Chemical Methodologies\u0026gt; and Library Synthesis\u003c\/em\u003e where she is also a project leader.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47989734113509,"sku":"NP9781119054160","price":139.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9781119054160.jpg?v=1761785294","url":"https:\/\/k12savings.com\/products\/organic-syntheses-volume-91-isbn-9781119054160","provider":"K12savings","version":"1.0","type":"link"}