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A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline. / Bakulina, Olga; Ivanov, Alexander; Suslonov, Vitalii; Darin, Dmitry; Krasavin, Mikhail.

в: Beilstein Journal of Organic Chemistry, Том 13, 18.07.2017, стр. 1413-1424.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Bakulina, O, Ivanov, A, Suslonov, V, Darin, D & Krasavin, M 2017, 'A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline', Beilstein Journal of Organic Chemistry, Том. 13, стр. 1413-1424. https://doi.org/10.3762/bjoc.13.138

APA

Bakulina, O., Ivanov, A., Suslonov, V., Darin, D., & Krasavin, M. (2017). A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline. Beilstein Journal of Organic Chemistry, 13, 1413-1424. https://doi.org/10.3762/bjoc.13.138

Vancouver

Bakulina O, Ivanov A, Suslonov V, Darin D, Krasavin M. A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline. Beilstein Journal of Organic Chemistry. 2017 Июль 18;13:1413-1424. https://doi.org/10.3762/bjoc.13.138

Author

Bakulina, Olga ; Ivanov, Alexander ; Suslonov, Vitalii ; Darin, Dmitry ; Krasavin, Mikhail. / A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline. в: Beilstein Journal of Organic Chemistry. 2017 ; Том 13. стр. 1413-1424.

BibTeX

@article{17d9dcd218b34e56baf5d076178ea8ff,
title = "A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline",
abstract = "A series of 15 benzene-fused hexahydropyrrolo[1,2-b]isoquinolonic acids with substantial degree of steric encumbrance has been prepared via a novel variant of the Castagnoli-Cushman reaction of homophthalic anhydride (HPA) and various indolenines. The employment of a special kind of a cyclic imine component reaction allowed, for the first time, isolating a Mannich-type adduct between HPA and an imine component which has been postulated but never obtained in similar reactions.",
keywords = "Castagnoli-Cushman reaction, Diastereoselectivity, Homophthalic anhydride, Indolenines, Lactam synthesis, Multicomponent reactions",
author = "Olga Bakulina and Alexander Ivanov and Vitalii Suslonov and Dmitry Darin and Mikhail Krasavin",
year = "2017",
month = jul,
day = "18",
doi = "10.3762/bjoc.13.138",
language = "English",
volume = "13",
pages = "1413--1424",
journal = "Beilstein Journal of Organic Chemistry",
issn = "2195-951X",
publisher = "Beilstein-Institut Zur Forderung der Chemischen Wissenschaften",

}

RIS

TY - JOUR

T1 - A speedy route to sterically encumbered, benzene-fused derivatives of privileged, naturally occurring hexahydropyrrolo[1,2-b]isoquinoline

AU - Bakulina, Olga

AU - Ivanov, Alexander

AU - Suslonov, Vitalii

AU - Darin, Dmitry

AU - Krasavin, Mikhail

PY - 2017/7/18

Y1 - 2017/7/18

N2 - A series of 15 benzene-fused hexahydropyrrolo[1,2-b]isoquinolonic acids with substantial degree of steric encumbrance has been prepared via a novel variant of the Castagnoli-Cushman reaction of homophthalic anhydride (HPA) and various indolenines. The employment of a special kind of a cyclic imine component reaction allowed, for the first time, isolating a Mannich-type adduct between HPA and an imine component which has been postulated but never obtained in similar reactions.

AB - A series of 15 benzene-fused hexahydropyrrolo[1,2-b]isoquinolonic acids with substantial degree of steric encumbrance has been prepared via a novel variant of the Castagnoli-Cushman reaction of homophthalic anhydride (HPA) and various indolenines. The employment of a special kind of a cyclic imine component reaction allowed, for the first time, isolating a Mannich-type adduct between HPA and an imine component which has been postulated but never obtained in similar reactions.

KW - Castagnoli-Cushman reaction

KW - Diastereoselectivity

KW - Homophthalic anhydride

KW - Indolenines

KW - Lactam synthesis

KW - Multicomponent reactions

UR - http://www.scopus.com/inward/record.url?scp=85025585812&partnerID=8YFLogxK

U2 - 10.3762/bjoc.13.138

DO - 10.3762/bjoc.13.138

M3 - Article

AN - SCOPUS:85025585812

VL - 13

SP - 1413

EP - 1424

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

SN - 2195-951X

ER -

ID: 34635463