4000-520-616
欢迎来到免疫在线!(蚂蚁淘生物旗下平台)  请登录 |  免费注册 |  询价篮
主营:原厂直采,平行进口,授权代理(蚂蚁淘为您服务)
咨询热线电话
4000-520-616
当前位置: 首页 > 新闻动态 >
新闻详情
Sherburn, Michael - The Australian National University...
来自 : www.x-mol.com/university/facul 发布时间:2021-03-25

Four-Step Total Synthesis of Selaginpulvilin D M. J. Sowden, M. S. Sherburn Org. Lett. 2017, 19, 636-63. DOI: 10.1021/acs.orglett.6b03793Preparation of an Ion with the Highest Calculated Proton Affinity: Ortho-Diethynylbenzene Dianion B. L. J. Poad, N. D. Reed, C. S. Hansen, A. J. Trevitt, S. J. Blanksby, E. G. Mackay, M. S. Sherburn, B. Chan, L. Radom Chem. Sci. 2016, 7, 6245-6250. DOI: 10.1039/C6SC01726FDirect Cross-Couplings of Propargylic Diols N. J. Green, A. C. Willis, and M. S. Sherburn Angew. Chem. Int. Ed. 2016, 55,9244 –9248. DOI: 10.1002/anie.201604527Synthesis and Diels–Alder Reactivity of Substituted [4]Dendralenes M. F. Saglam, A. R. Alborzi, A. D. Payne, A. C. Willis, M. N. Paddon-Row, and M. S. Sherburn J. Org. Chem., 2016, 81, 1461-1475. DOI: 10.1021/acs.joc.5b02583Multicomponent diene-transmissive Diels-Alder sequences featuring aminodendralenes S. M. Tan, A. C. Willis, M. N. Paddon-Row and M. S. Sherburn Angew. Chem. Int. Ed. 2016, 55, 3081–3085. DOI: 10.1002/anie.201510925Discovery and Computational Rationalization of Diminishing Alternation in [n]Dendralenes M. F. Saglam, T. Fallon, M. N. Paddon-Row, and M. S. Sherburn J. Am. Chem. Soc., 2016, 138, 1022-1032. DOI: 10.1021/jacs.5b11889A Domino Diels–Alder Approach toward the Tetracyclic Nicandrenone Framework E. G. Mackay, M. Nörret, L. S.-M. Wong, I. Louis, A. L. Lawrence, A. C. Willis, and M. S. Sherburn Org. Lett., 2105, 17, 5517–5519. DOI: 10.1021/acs.orglett.5b02412[5]Radialene E. G. Mackay, C. G. Newton, H. Toombs-Ruane, E. J. Lindeboom, T. Fallon, A. C. Willis, M. N. Paddon-Row, and M. S. Sherburn J. Am. Chem. Soc., 2015, 137, 14653–14659. DOI: 10.1021/jacs.5b07445 Featured on the cover.Preparation and Synthetic Value of π-Bond Rich Branched Hydrocarbons M. S. Sherburn Acc. Chem. Res., 2015, 48, 1961–1970. DOI: 10.1021/acs.accounts.5b00242Unified Total Synthesis of the Natural Products Endiandric Acid A, Kingianic Acid E, and Kingianins A, D and F S. L. Drew, A. L. Lawrence and M. S. Sherburn Chemical Science, 2015, 6, 3886 – 3890. DOI: 10.1039/C5SC00794ATotal synthesis of the pseudopterosin aglycones C. G. Newton and M. S. Sherburn Nat. Prod. Rep., 2015, 32, 865-876. DOI: 10.1039/C5NP00008DTotal Synthesis of Ramonanins A–D R. S. Harvey, E. G. Mackay, L. Roger, M. N. Paddon-Row, M. S. Sherburn, A. L. Lawrence Angew. Chem. Int. Ed., 2015, 54, 1795–1798. DOI: 10.1002/anie.201409818A Combined Computational-Experimental Study of the Kinetics of Intramolecular Diels–Alder Reactions in a Series of 1,3,8-Nonatrienes.W. J. Lording, A. D. Payne, T. N. Cayzer, M. S. Sherburn, M. N. Paddon-Row Aust. J. Chem. (special issue dedicated to the memory of Dr Des Brown), 2015, 68, 230–240. DOI: 10.1071/CH14430Pseudopterosin synthesis from a chiral cross-conjugated hydrocarbon through a series of cycloadditions C. G. Newton, S. L. Drew, A. L. Lawrence, A. C. Willis, M N. Paddon-Row, M. S. Sherburn Nat. Chem. 2015, 7, 82–86 DOI: 10.1038/nchem.2112The Diels–Alder Reaction in Steroid Synthesis E. G. Mackay, M. S. Sherburn Synthesis, 2015, 47, 1–21 DOI: 10.1055/s-0034-1378676Computational and Synthetic Studies with Tetravinylethylenes E. J. Lindeboom, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn J. Org. Chem., 2014, 79, 11496–11507. DOI: 10.1021/jo5021294Simple Synthetic Receptors for Aspirin T. V. Nguyen, M. S. Sherburn Chem. Eur. J., 2014, 20, 14991–14995 DOI: 10.1002/chem.201304808Tetravinylethylene.E. J. Lindeboom, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn Angew. Chem. Int. Ed. 2014, 53, 5440-5443 DOI: 10.1002/anie.201402840Furanodendralenes.T. Fallon, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn J. Org. Chem. 2014, 79, 3185-3193 DOI: 10.1021/jo500458yTotal Synthesis and Structural Revision of the Alkaloid Incargranine B.P. D. Brown, A. C. Willis, M. S. Sherburn, A. L. Lawrence Angew. Chem. Int. Ed. 2013, 52, 13273-13275 DOI: 10.1002/anie.201307875

本文链接: http://sherchem.immuno-online.com/view-719475.html

发布于 : 2021-03-25 阅读(0)
公司介绍
品牌分类
催化剂和助剂 Others
联络我们
服务热线:4000-520-616
(限工作日9:00-18:00)
QQ :1570468124
手机:18915418616