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    1. Ni/Photoredox-Catalyzed Enantioselective Acylation of α‑Bromobenzoates with Aldehydes: (...)

      http://duke.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3JbhQxELUgHOBC2ASdAHKkcEJOum1PtxtFkYZWRogDIixCnFpeM5GiaUTPSJmc8gv8Az_Aj_ARfAlVvQyTgYjceqleXC67Xtm1ELJttcyNi3PmEu2ZFAHmQR5nTA_i1KbSaBtjNPIn9fozP3ynRksOsqs7-BzzA9l6R1oQvlReJzd4CgoUIVDx_k_8I1dJD3MzlYrOwX31aVRAtr6ogP5Clf9UQI2yGa2Twz5kp_G03mk9Tdo1hwsu2Eu5HP_Tojvkdoc86bAVlbvkmp_cIzeLvuDbffL9zfHu23EFRrh31SkrcGFnfuYdPUBnmeOqbkrmwOxIh3beutDRKtCfP36df3uJXn3GT84qxK4UV3fp3nh_eOL8eO58vbc73n9Bh3SEEBl-ostkTqfVMhlSsZVzWiAbWVHNMHb46AH5ODr4ULxiXREHpgGrTZkL3iiRJjp3WFsdAIHl1sBBLoOWwvgAiE_4kA9C4NYZkQVQl5lOBlbC5JCKR4QmLjbBS2-CBIPOmlxpC0DXDeATmYxFRLaApWU3-uqy2VjnYNjg1Y7REXned3tpu_TnWIXj5BLqZwvqL23aj0votnoJKqG3cLNFT3w1q0sRg-mMwX5ZRB62orV4k1AKGJGriGwvy9riPmJQCZayypvNl4gkVyErulZhMoPpxhVYsklucYBouFLN5WOyNv0680_aohhPmwH2GxgHIsc

      by Cheng, Junliang; Zu, Weisai; Huang, Yongliang; Huo, Haohua; Li, Chengyang; Wan, Xiang; Xu, Yumin and Li, Jian

      Journal Of The American Chemical Society, Volume 146, Issue 29, pp. 19909 - 19918

      Journal Article : Full Text Online

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    2. N‑Acetylcysteine: Antioxidant, Aldehyde Scavenger, and More

      http://duke.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1fSxtBEB_EvhSKrbZotJYtiC_Nmb3dvX9FhBAbpNBiq6WKD8f-O09IE0kimDe_Qr9iP0lnby9J0yLa17udhZud3fntzcxvAHa0FJkyNAtMKG0geIHnIKNJICMa61goqamrRv6efjxnX76m3c4S0Hsi-CxsSY3KL-0P16picLuXVW4eD90nLEZX6sBQ52QWN0AJz-2Z8YCx9GxaE3zvPM4p6dGiU_oHaf6dMOlTJSsP1H0OF9M6nir9es-nn_gfEQt52X8QPD76M1_ASg1MSdtb0ios2f4a7B57ZutJk5zOC7VGTbJLjuec15M1eOZ__xFf1fQSDj__uvvZ1nY86WnHFY1Y9j1pu8zK2yuDi9kk--VBu2dsOTF2v1UekBPtGttf2mGTyL4hnwZD-wq-dT-cdo6CumEDLi3j48Di7axINKKAoohtlgml0kzaxBhpEoVITEaJLApuVSEUnsLoPyNH_2NEyqnlMd8AEhqqCivcELy8aZWlUiOoNZHkeIGmvAHvUFV5vdNGeRVEZ2HuHs71l9f6a0A0Xdhc16TnrvdG70G51kzu2tN-PCjxdmo3Oe5QF3aRfTu4GeWuYzqqJBa0AevejmZzchdiZyJuQLJgYbMBjv178U3_qqxYwPGml3Aebf6XPrbgKSI-V7YWhNFrWB4Pb-y274PxptpJvwHdMyS2

      by Zhitkovich, Anatoly

      Chemical Research In Toxicology, Volume 32, Issue 7, pp. 1318 - 1319

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    3. Salting‐Out Aldehyde from the Electrooxidation of Alcohols with 100 % Selectivity

      http://duke.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3Na9swFBell_XSdutgbrOhQctOXmTJnxACxiRsO6x02RiDgZFliZSGZCwJdLdcd9vf2L9k71m2Ex9GR3uz0ROW9PTxnvze70fIuZJ-UpQscUtPatcXBvZBziJXBixUoV9IxTAb-Wv84Ru_-hSPs50sfosP0V644cqo9mtc4LJY9regoZiBDf4d54hQhXCfCN2EFtJl1npcMDltepEQLrLQN6iNjPe71bun0tbU7BxGO_arqA-g8RG5aZpeRV-_tdEn9h6iE5bd4Ds-ppfH5LC2U2lqJ9ZTsqfnz8iTrKGHOyHfJ3KGIdN3mz-X6xUdTIfprNTTX6Ue9KdDimkrFIxLOrI8O4vba8veRBeGppaXd0nxFphCG-42vy_opKLkqcgsnpMv49Hn7J1bUzW4SgRMuFwZUHipQqPKUAWxJyMTmVCDvhPhF4nxfFMYUD54X540CLsXcYnYbqA140nxglCvZIXRvi4MSCWqSGKpwJwtAynAdWbCIW6jo1zVAObIozHLLfQyz3Gw8nawHPKmlf9hoTv-KdlrVJ7XS3iZg10HGxqLIih-3RbDIOMfFTnXizXKeOghx2HskPPdqdJ-sPIZwSVFGESwCBzi_Y9YVncPcQlWDuHVDLmnE3n68f2ofTt9SKUzcoDPVapl1CP7q59r_dKyZLyqFtZflYsjqg

      by Chen, Wei; Xu, Leitao; Wu, Jingcheng; Lu, Yuxuan; Zou, Yuqin; Wu, Yandong; Wang, Shuangyin; Yang, Ming; Pan, Yuping; Huang, Zhifeng et al.

      Angewandte Chemie International Edition, Volume 61, Issue 45.

      Journal Article : Full Text Online

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    1. Aldehyde

      https://find.library.duke.edu/catalog/DUKE000541264

      hrsg. von Jürgen Falbe ; bearbeitet von H. Bach ... [et al.]

      Book

      Check Holdings for this item's availability Perkins & Bostock Library, QD258 .M44 1982 4. Aufl., Erwbd., Bd.3 

    2. Aldehyde Dehydrogenases : From Alcohol Metabolism to Human Health and Precision Medicine

      https://find.library.duke.edu/catalog/DUKE99119246877808501

      edited by Jun Ren, Yingmei Zhang, Junbo Ge.

      Book : View Online

      cover thumbnail

    3. Alcohol and aldehyde metabolizing systems, IV

      https://find.library.duke.edu/catalog/DUKE000412048

      edited by Ronald G. Thurman.

      Book

      Check Holdings for this item's availability Medical Center Library, QV82 In8p 1979 c.1

      cover thumbnail

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    1. https://library.duke.edu/sites/default/files/dul/users/arianne.hartsellgundy/natural_products_ (...)

      https://library.duke.edu/sites/default/files/dul/users/arianne.hartsellgundy/natural_products_s_kwartler.pdf

      As for this, I can’t decide SHACHAR That could be an aldehyde. SASSON Tov, I think you should try again But with your sample more purified.

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    1. Aromatic aldehydes and carbinols as carbon monoxide donors.

      https://find.library.duke.edu/catalog/DUKE004148119

      Archival and manuscript material

      Check Holdings for this item's availability Library Service Center, N3419 no.1679 

    2. The action of alkali on [delta]³-cyclohexene aldehydes

      https://find.library.duke.edu/catalog/DUKE004147315

      by Dudley M. Gallagher.

      Archival and manuscript material, Book

      This item is currently Available Library Service Center, N3419 no.463 c.1

    3. Optical studies on some crystalline organic compounds: I. Nitrogen substituted (...)

      https://find.library.duke.edu/catalog/DUKE004165628

      Archival and manuscript material

      This item is currently Available Library Service Center, N3419 no.642 

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