A short route to 2,3-dimethylene-7-oxabenzonorbornenes

1989 ◽  
Vol 54 (7) ◽  
pp. 1762-1764 ◽  
Author(s):  
Jihmei Luo ◽  
Harold Hart
Keyword(s):  
2020 ◽  
Vol 17 (7) ◽  
pp. 588-591
Author(s):  
Pingxuan Shao ◽  
Wei Lu ◽  
Lei Wang

A practical and concise total synthesis of tricyclic ketone 7 (CDE ring), a valuable intermediate for the synthesis of racemic camptothecin and analogs, was described (8 chemical steps and 29% overall yield). The synthesis starts with two inexpensive, readily available materials and is operationally simple to perform. It is worth mentioning that the reported protecting group-free synthesis, with advantages of a short route, would be helpful for the future development of industry-scale syntheses of camptothecin-family alkaloids.


ChemInform ◽  
2010 ◽  
Vol 41 (35) ◽  
pp. no-no
Author(s):  
Fedor I. Zubkov ◽  
Inga K. Airiyan ◽  
Anastasiya A. Dzyubenko ◽  
Nataliya I. Yudina ◽  
Vladimir P. Zaytsev ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 33 (38) ◽  
pp. no-no
Author(s):  
Edward P. Serebryakov ◽  
Galina D. Gamalevich ◽  
Veacheslav N. Kulcitki ◽  
Nicon D. Ungur ◽  
Pavel F. Vlad

ChemInform ◽  
2012 ◽  
Vol 43 (5) ◽  
pp. no-no
Author(s):  
Soraya Manaviazar ◽  
Karl J. Hale

ChemInform ◽  
2010 ◽  
Vol 33 (22) ◽  
pp. no-no
Author(s):  
Iben Damager ◽  
Carl Erik Olsen ◽  
Birger Lindberg Moeller ◽  
Mohammed Saddik Motawia
Keyword(s):  

Heterocycles ◽  
1980 ◽  
Vol 14 (6) ◽  
pp. 827 ◽  
Author(s):  
Maurice Shamma ◽  
G. Manikumar ◽  
M. Shamma
Keyword(s):  

Synthesis ◽  
2020 ◽  
Author(s):  
Zbigniew Wróbel ◽  
Michał Tryniszewski ◽  
Robert Bujok ◽  
Roman Gańczarczyk

Tributyl- or triphenylphosphine promotes a one-pot, three-step method for the synthesis of differently substituted dibenzodiazepinones from N-aryl-2-nitroanilines. Pyridine analogues and the corresponding thiazepinones can also be formed using this method. The process involves deoxygenation of the nitro group, then formation of an iminophosphorane intermediate and its intramolecular condensation with a carboxyl group placed in the N-aryl group. The role of the carboxyl group in the formation of the iminophosphorane and the mode of cyclization are discussed.


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