Photo-induced elimination in some aporphinium salts

1978 ◽  
Vol 31 (2) ◽  
pp. 313 ◽  
Author(s):  
JB Bremner ◽  
KN Winzenberg

Ultraviolet irradiation of (+)-glaucine methiodide in methanol gave the elimination product 1-[2'-(N,N-dimethylaminoethyl)]-3,4,6,7- tetramethoxyphenanthrene in good yield. Analogous products were obtained from the ethiodide and benzylbromide salts of this aporphine alkaloid, and from quaternary salts of (+)-boldine and (-)-O,O'-dimethylapomorphine. This photoelimination reaction was also applied to the hydrochloride salts of (+)-glaucine and (+)-boldine.

1970 ◽  
Vol 48 (12) ◽  
pp. 1948-1950 ◽  
Author(s):  
G. W. Shaffer

Ultraviolet irradiation of β-bromo-β-nitrostyrene in hydroxylic solvents gives a good yield of alkyl α-isonitrosophenyl acetates (1).


2013 ◽  
Vol 133 (1) ◽  
pp. 13-19
Author(s):  
Kotaro Rokkaku ◽  
Fumiaki Fukawa ◽  
Susumu Suzuki ◽  
Haruo Itoh

1970 ◽  
Author(s):  
J. HAYES ◽  
R. KROES ◽  
A. KULSHRESHTHA ◽  
T. MOOKHERJI ◽  
U. WEGNER

2019 ◽  
Author(s):  
Tristan Delcaillau ◽  
Alessandro Bismuto ◽  
Zhong Lian ◽  
Bill Morandi

A nickel-catalyzed carbon-sulfur bond metathesis has been developed to access high-value thioethers. 1,2-bis(dicyclohexylphosphino)ethane (dcype) is essential to promote this highly functional group tolerant reaction. Further, synthetically challenging macrocycles could be obtained in good yield in an unusual example of ring-closing metathesis which does not involve alkene bonds. In-depth organometallic studies support a reversible Ni(0)-Ni(II) pathway to product formation. Overall, this work does not only disclose a more sustainable and more functional group tolerant alternative to previous catalytic systems based on Pd, but also presents new applications and mechanistic information which are highly relevant to the further development and application of unusual single bond metathesis reactions.


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