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Open access
Beilstein-Institut
Beilstein Journal of Organic Chemistry
,  том 9 ,  страницы 1601-1606

Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition

Тип публикации: Journal Article
Дата публикации: 2013-08-06
Beilstein-Institut
scimago Q2
wos Q3
БС2
SJR: 0.482
CiteScore: 3.8
Impact factor: 2.1
ISSN: 18605397
Organic Chemistry
Краткое описание

Katsumadain A, a naturally occurring influenza virus neuraminidase (NA) inhibitor, was synthesized by using a bioinspired, organocatalytic enantioselective 1,4-conjugate addition of styryl-2-pyranone with cinnamaldehyde, followed by a tandem Horner–Wadsworth–Emmons/oxa Michael addition.

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Wang Y. et al. Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition // Beilstein Journal of Organic Chemistry. 2013. Vol. 9. pp. 1601-1606.
ГОСТ со всеми авторами (до 50) Скопировать
Wang Y., Tang Y. Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition // Beilstein Journal of Organic Chemistry. 2013. Vol. 9. pp. 1601-1606.
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TY - JOUR
DO - 10.3762/bjoc.9.182
UR - https://doi.org/10.3762/bjoc.9.182
TI - Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition
T2 - Beilstein Journal of Organic Chemistry
AU - Wang, Yongguang
AU - Tang, Yefeng
PY - 2013
DA - 2013/08/06
PB - Beilstein-Institut
SP - 1601-1606
VL - 9
PMID - 23946860
SN - 1860-5397
ER -
BibTex
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@article{2013_Wang,
author = {Yongguang Wang and Yefeng Tang},
title = {Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition},
journal = {Beilstein Journal of Organic Chemistry},
year = {2013},
volume = {9},
publisher = {Beilstein-Institut},
month = {aug},
url = {https://doi.org/10.3762/bjoc.9.182},
pages = {1601--1606},
doi = {10.3762/bjoc.9.182}
}