Self-immolative asymmetric synthesis in the allylic rearrangement of an optically active amine oxide
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1970/C2/C29700000419
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis and photochemical response of Ru(ii)-coordinated double-decker silsesquioxane;RSC Advances;2018
2. Chiral t-butylphenylphosphinothioic acid in NMR analysis of tertiary amine oxides with a stereogenic nitrogen atom;Tetrahedron: Asymmetry;1997-07
3. Asymmetric synthesis of (R)-hexane-1,5-diol and (R)-hex-3-ene-1,5-diol via a tandem asymmetric conjugate addition / stereospecific meisenheimer rearrangement protocol;Tetrahedron: Asymmetry;1996-04
4. Asymmetric synthesis of (R)-hexane-1,5-diol, (R)-hex-3-ene-1,5-diol and (R)-6-methylhept-5-en-2-ol (sulcatol) employing a tandem asymmetric conjugate addition and stereospecific Meisenheimer rearrangement protocol;Journal of the Chemical Society, Perkin Transactions 1;1996
5. An Efficient Route to Both Enantiomers ofN-(p-Tolylsulfonyl)benzenesulfonimidamide and Their Use for Asymmetric Allylic Amination of Olefins;Bulletin of the Chemical Society of Japan;1989-04-15
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