Selective acylation of a sterically hindered hydroxyl group of unsymmetrical diols containing a primary hydroxyl group such as 1,5-hexanediol in the presence of silica gel with acetyl chloride

2003 ◽  
Vol 16 (6) ◽  
pp. 355-358 ◽  
Author(s):  
Haruo Ogawa ◽  
Yuko Ide ◽  
Ryoichi Honda ◽  
Teiji Chihara

ACS Catalysis ◽  
2017 ◽  
Vol 7 (9) ◽  
pp. 6150-6154 ◽  
Author(s):  
Yasunori Toda ◽  
Tomoyuki Sakamoto ◽  
Yutaka Komiyama ◽  
Ayaka Kikuchi ◽  
Hiroyuki Suga


1967 ◽  
Vol 15 (6) ◽  
pp. 894-896 ◽  
Author(s):  
Takuma Sasaki ◽  
Yoshihisa Mizuno


2009 ◽  
Vol 344 (4) ◽  
pp. 501-506 ◽  
Author(s):  
Sayuri Yonekawa ◽  
Clifford A. Lingwood ◽  
Murugesapillai Mylvaganam


Author(s):  
�. G. Rozantsev ◽  
G. L. Grigoryan ◽  
V. P. Ivanov


1952 ◽  
Vol 30 (9) ◽  
pp. 627-645 ◽  
Author(s):  
O. E. Edwards ◽  
Léo Marion

The ultraviolet spectra, basic strengths, and N-alkyl groups of the aconite alkaloids are discussed. Pyropseudaconine has been shown to contain a conjugated system. The formulation C19H19–2,(OH)3,(OCH3)4NC2H5 has been confirmed for lycoctonine. Study of its oxidation products has shown that lycoctonine has a methylene group adjacent to the nitrogen and a primary hydroxyl group. The two remaining hydroxyls have been shown to be vicinal, with one probably secondary and the other tertiary. A carbinolamine structure is suggested for hydroxylycoctonine. The new bases, isolycoctonine, desoxylycoctonine, and des-(oxymethylene)-lycoctonine are described.





1962 ◽  
Vol 34 (9) ◽  
pp. 1147-1150 ◽  
Author(s):  
W. B. Crummett


ChemInform ◽  
2010 ◽  
Vol 23 (1) ◽  
pp. no-no
Author(s):  
K. YOSHINAGA ◽  
M. RIKITAKE ◽  
T. KITO ◽  
Y. YAMAMOTO ◽  
H. EGUCHI ◽  
...  


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