Urea as an organic solvent and reagent for the addition/cyclization/ fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids

Denis S. Baranov, Sergei F. Vasilevsky, Brian Gold, Igor V. Alabugin

Результат исследований: Материалы для журнала › Статья › рецензирование

Аннотация

Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10- anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones - substituted analogues of Aporphinoid alkaloids.

Язык оригинала	Английский
Страницы (с-по)	1745-1750
Число страниц	6
Журнал	RSC Advances
Том	1
Номер выпуска	9
DOI	https://doi.org/10.1039/c1ra00622c
Состояние	Опубликовано - 7 дек 2011
Опубликовано для внешнего пользования	Да

ASJC Scopus subject areas

Chemical Engineering(all)
Chemistry(all)

Доступ к документу

10.1039/c1ra00622c

Другие файлы и ссылки

Fingerprint Подробные сведения о темах исследования «Urea as an organic solvent and reagent for the addition/cyclization/ fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids». Вместе они формируют уникальный семантический отпечаток (fingerprint).

Цитировать

Urea as an organic solvent and reagent for the addition/cyclization/ fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids. / Baranov, Denis S.; Vasilevsky, Sergei F.; Gold, Brian; Alabugin, Igor V.

В: RSC Advances, Том 1, № 9, 07.12.2011, стр. 1745-1750.

Результат исследований: Материалы для журнала › Статья › рецензирование

@article{77055f599d29433f956da22089732ab1,

title = "Urea as an organic solvent and reagent for the addition/cyclization/ fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids",

abstract = "Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10- anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones - substituted analogues of Aporphinoid alkaloids.",

author = "Baranov, {Denis S.} and Vasilevsky, {Sergei F.} and Brian Gold and Alabugin, {Igor V.}",

year = "2011",

month = dec,

day = "7",

doi = "10.1039/c1ra00622c",

language = "English",

volume = "1",

pages = "1745--1750",

journal = "RSC Advances",

issn = "2046-2069",

publisher = "Royal Society of Chemistry",

number = "9",

}

TY - JOUR

T1 - Urea as an organic solvent and reagent for the addition/cyclization/ fragmentation cascades leading to 2-R-7H-dibenzo[de,h]quinolin-7-one analogues of Aporphinoid alkaloids

AU - Baranov, Denis S.

AU - Vasilevsky, Sergei F.

AU - Gold, Brian

AU - Alabugin, Igor V.

PY - 2011/12/7

Y1 - 2011/12/7

N2 - Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10- anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones - substituted analogues of Aporphinoid alkaloids.

AB - Molten urea serves both as a solvent and a reagent for the one-pot addition/cyclizations/fragmentation cascade which converts peri-alkynyl-9,10- anthraquinones into 2-R-7H-dibenzo[de,h]quinolin-7-ones - substituted analogues of Aporphinoid alkaloids.

UR - http://www.scopus.com/inward/record.url?scp=84859147934&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84859147934&partnerID=8YFLogxK

U2 - 10.1039/c1ra00622c

DO - 10.1039/c1ra00622c

M3 - Article

AN - SCOPUS:84859147934

VL - 1

SP - 1745

EP - 1750

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

IS - 9

ER -