Standard

Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity. / Kulyashova, Alexandra; Krasavin, Mikhail.

In: Tetrahedron Letters, Vol. 57, No. 39, 2016, p. 4395-4397.

Research output: Contribution to journal › Article › peer-review

Harvard

Kulyashova, A & Krasavin, M 2016, 'Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity', Tetrahedron Letters, vol. 57, no. 39, pp. 4395-4397. <http://www.sciencedirect.com/science/article/pii/S0040403916310863>

APA

Kulyashova, A., & Krasavin, M. (2016). Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity. Tetrahedron Letters, 57(39), 4395-4397. http://www.sciencedirect.com/science/article/pii/S0040403916310863

Vancouver

Kulyashova A, Krasavin M. Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity. Tetrahedron Letters. 2016;57(39):4395-4397.

Author

Kulyashova, Alexandra ; Krasavin, Mikhail. / Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity. In: Tetrahedron Letters. 2016 ; Vol. 57, No. 39. pp. 4395-4397.

BibTeX

@article{49c7f8e09d6247a0a6a047673c120109,
title = "Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity",
abstract = "An efficient modular approach toward medicinally important 5-acylamino-4,5-isoxazolines via the 1,3-dipolar cycloaddition reaction of nitrile oxides and MCR-derived enamide building blocks is described. This approach results in isoxazolines containing four elements of diversity utilizing two practically simple synthetic operations.",
author = "Alexandra Kulyashova and Mikhail Krasavin",
year = "2016",
language = "English",
volume = "57",
pages = "4395--4397",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "39",

}

RIS

TY - JOUR

T1 - Convenient modular construction of medicinally important 5-acylamino-4,5-dihydroisoxazoles featuring four elements of diversity

AU - Kulyashova, Alexandra

AU - Krasavin, Mikhail

PY - 2016

Y1 - 2016

N2 - An efficient modular approach toward medicinally important 5-acylamino-4,5-isoxazolines via the 1,3-dipolar cycloaddition reaction of nitrile oxides and MCR-derived enamide building blocks is described. This approach results in isoxazolines containing four elements of diversity utilizing two practically simple synthetic operations.

AB - An efficient modular approach toward medicinally important 5-acylamino-4,5-isoxazolines via the 1,3-dipolar cycloaddition reaction of nitrile oxides and MCR-derived enamide building blocks is described. This approach results in isoxazolines containing four elements of diversity utilizing two practically simple synthetic operations.

M3 - Article

VL - 57

SP - 4395

EP - 4397

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 39

ER -

ID: 7583318