Microwave-assisted aza-Prins reaction. Part 2: Straightforward access to 2,6-disubstituted 1-azaadamantanes

V. Parchinsky; A. Shumsky; M. Krasavin

Статья

Microwave-assisted aza-Prins reaction. Part 2: Straightforward access to 2,6-disubstituted 1-azaadamantanes

V. Parchinsky, A. Shumsky, M. Krasavin,

2021

https://doi.org/10.1016/j.tetlet.2011.10.125

Novel symmetrically and unsymmetrically disubstituted 1-azaadamantanes were prepared as a single, chiral diastereomer via double microwave-assisted aza-Prins cyclization in one-pot or sequential reaction format. © 2011 Elsevier B.V. All rights reserved.

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1. Version of Record от 2021-04-27

Метаданные

Об авторах

V. Parchinsky
Chemical Diversity Research Institute, 2a Rabochaya St., Khimki, Moscow Reg. 141400, Russian Federation
A. Shumsky
Science and Education Center Innovative Research, Yaroslavl State Pedagogical University, Yaroslavl 150000, Russian Federation
M. Krasavin
Eskitis Institute, Griffith University, Brisbane, QLD 4111, Australia

Название журнала

Tetrahedron Letters

Том

Выпуск

Страницы

7161-7163

Ключевые слова

1 azaadamantane; adamantane derivative; unclassified drug; article; chirality; cyclization; diastereoisomer; microwave radiation; one pot synthesis

Тип документа

journal article

Источник

scopus

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Статья

Microwave-assisted aza-Prins reaction. Part 2: Straightforward access to 2,6-disubstituted 1-azaadamantanes

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