New synthesis of 2-exo-brendanol
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo01287a085
Cited by 16 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. Azabrendanes. III. Synthesis of stereoisomeric exo- and endo-5-acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and their reduction by lithium aluminum hydride;Heteroatom Chemistry;2001
2. Observations on the state of synthesis: Some magic moments revisited;Tetrahedron;1997-06
3. Azabrendanes. II. Chemo-, regio- and stereoselective transformation of 3-oxatricyclo[3.2.1.02,4]octane-endo-6-carbonitrile in reaction with lithium aluminum hydride;Heteroatom Chemistry;1997
4. Direct access to substituted brendane derivatives by palladium-copper mediated cyclisation of endo-5-vinyl-2-norbornene. X-ray structure of the σ-π intermediate palladium complex. Further evolution (Baeyer-Villiger oxidation) to the quinane system;Tetrahedron;1994-01
5. Single electron transfer in metal halogen exchange. The reaction of organolithium compounds with alkyl halides;The Journal of Organic Chemistry;1987-04
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