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Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines. / Эрхитуева, Елена Баировна; Паникоровский, Тарас Леонидович; Svintsitskaya, N I; Трифонов, Ростислав Евгеньевич; Dogadina, A V.

в: Synlett, Том 29, № 7, 23.04.2018, стр. 933-937.

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

Harvard

Эрхитуева, ЕБ, Паникоровский, ТЛ, Svintsitskaya, NI, Трифонов, РЕ & Dogadina, AV 2018, 'Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines', Synlett, Том. 29, № 7, стр. 933-937. https://doi.org/10.1055/s-0036-1591919

APA

Эрхитуева, Е. Б., Паникоровский, Т. Л., Svintsitskaya, N. I., Трифонов, Р. Е., & Dogadina, A. V. (2018). Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines. Synlett, 29(7), 933-937. https://doi.org/10.1055/s-0036-1591919

Vancouver

Эрхитуева ЕБ, Паникоровский ТЛ, Svintsitskaya NI, Трифонов РЕ, Dogadina AV. Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines. Synlett. 2018 Апр. 23;29(7):933-937. https://doi.org/10.1055/s-0036-1591919

Author

Эрхитуева, Елена Баировна ; Паникоровский, Тарас Леонидович ; Svintsitskaya, N I ; Трифонов, Ростислав Евгеньевич ; Dogadina, A V. / Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines. в: Synlett. 2018 ; Том 29, № 7. стр. 933-937.

BibTeX

@article{307f99df1cf54867ac6457a76eedc9bc,
title = "Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines",
abstract = "An efficient synthesis of a series of novel symmetrical N- aryl- C -phosphonoacetamidines through reaction of diisopropyl (chloroethynyl)phosphonate with primary aryl amines was developed. This procedure tolerates a wide range of functional groups and has a good atom economy. The (E) - isomer was the major product that crystallized preferentially over the (Z)-isomer.",
keywords = "aryl amidines, aryl amines, carbamimidoylphosphonoacetic acid, phosphonoacetamidines, COORDINATION CHEMISTRY, AMIDINES, ARYLAMIDINES, PHOSPHONATES, LIGANDS, AMINES, GUANIDINES, BIOLOGICAL EVALUATION, INHIBITORS, ACETAMIDINES",
author = "Эрхитуева, {Елена Баировна} and Паникоровский, {Тарас Леонидович} and Svintsitskaya, {N I} and Трифонов, {Ростислав Евгеньевич} and Dogadina, {A V}",
year = "2018",
month = apr,
day = "23",
doi = "10.1055/s-0036-1591919",
language = "English",
volume = "29",
pages = "933--937",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "7",

}

RIS

TY - JOUR

T1 - Synthesis of Symmetrical N- Aryl- C- phosphonoacetamidines

AU - Эрхитуева, Елена Баировна

AU - Паникоровский, Тарас Леонидович

AU - Svintsitskaya, N I

AU - Трифонов, Ростислав Евгеньевич

AU - Dogadina, A V

PY - 2018/4/23

Y1 - 2018/4/23

N2 - An efficient synthesis of a series of novel symmetrical N- aryl- C -phosphonoacetamidines through reaction of diisopropyl (chloroethynyl)phosphonate with primary aryl amines was developed. This procedure tolerates a wide range of functional groups and has a good atom economy. The (E) - isomer was the major product that crystallized preferentially over the (Z)-isomer.

AB - An efficient synthesis of a series of novel symmetrical N- aryl- C -phosphonoacetamidines through reaction of diisopropyl (chloroethynyl)phosphonate with primary aryl amines was developed. This procedure tolerates a wide range of functional groups and has a good atom economy. The (E) - isomer was the major product that crystallized preferentially over the (Z)-isomer.

KW - aryl amidines

KW - aryl amines

KW - carbamimidoylphosphonoacetic acid

KW - phosphonoacetamidines

KW - COORDINATION CHEMISTRY

KW - AMIDINES

KW - ARYLAMIDINES

KW - PHOSPHONATES

KW - LIGANDS

KW - AMINES

KW - GUANIDINES

KW - BIOLOGICAL EVALUATION

KW - INHIBITORS

KW - ACETAMIDINES

UR - http://www.scopus.com/inward/record.url?scp=85041832085&partnerID=8YFLogxK

UR - http://www.mendeley.com/research/synthesis-symmetrical-n-aryl-c-phosphonoacetamidines

U2 - 10.1055/s-0036-1591919

DO - 10.1055/s-0036-1591919

M3 - Article

VL - 29

SP - 933

EP - 937

JO - Synlett

JF - Synlett

SN - 0936-5214

IS - 7

ER -

ID: 35404590