Synthesis of condensed pregnano[17,16-d]triazolines under high pressure


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Abstract

Condensed pregnano[17,16-d]triazolines were produced in 1,3-dipolar cycloaddition of 16-dehydropregnenolone acetate with organic azides at 10 kbar. The structure of the synthesized compounds was determined by using two-dimensional NMR spectroscopy (1H—1H COSY, NOESY, HSQC, and HMBC).

About the authors

I. P. Sedishev

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

A. A. Zharov

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

I. S. Levina

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

A. Yu. Tyurin

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

Yu. A. Volkova

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

A. N. Aksenov

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

V. V. Kachala

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

T. A. Tikhonova

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

I. V. Zavarzin

N. D. Zelinsky Institute of the Organic Chemistry, Russian Academy of Sciences

Author for correspondence.
Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991


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