Reinvestigation of dimerization of Z-N-alkylarylmethylideneindoxyls upon exposure to UV-vis radiation


Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

N-Alkyl-2-arylmethylideneindoxyls upon exposure to UV or visible light undergo dimerization not to cyclobutane adducts as it has been reported earlier, but to spiropyrano[3,2-b]-pseudoindoxyls with a spiropseudoindoxyl fragment characteristic of many natural alkaloids. The structure of spiropyranopseudoindoxyls was established by NMR spectroscopy and X-ray crystallography.

Авторлар туралы

O. Babii

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

A. Hodak

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

A. Peregudov

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

V. Polshakov

Department of Fundamental Medicine, M. V. Lomonosov Moscow State University

Email: vel@ineos.ac.ru
Ресей, 1 Leninskie Gory, Moscow, 119991

Z. Starikova

Email: vel@ineos.ac.ru

Yu. Borisov

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

Yu. Fedorov

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

V. Velezheva

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: vel@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

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