Elsevier
Tetrahedron Letters
,  том 39 ,  издание 37 ,  страницы 6651-6654

Bilane synthesis through bilene-a: An alternative approach

Тип публикации: Journal Article
Дата публикации: 1998-09-01
Elsevier
scimago Q3
wos Q3
БС2
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
An alternative approach to bilanes has been developed which involves reduction of a bilene-a derivative with an unprotected terminal α position. The required bilene-a was constructed by acid-catalyzed condensation of an appropriate tripyrrane carboxylic acid with a formylpyrrole. The new route is demonstrated by the syntheses of aminomethylbilane and 18-butyrate aminomethylbilane.
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ГОСТ |
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Xue T., Alan J. Scott A. Bilane synthesis through bilene-a: An alternative approach // Tetrahedron Letters. 1998. Vol. 39. No. 37. pp. 6651-6654.
ГОСТ со всеми авторами (до 50) Скопировать
Xue T., Alan J. Scott A. Bilane synthesis through bilene-a: An alternative approach // Tetrahedron Letters. 1998. Vol. 39. No. 37. pp. 6651-6654.
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TY - JOUR
DO - 10.1016/S0040-4039(98)01426-9
UR - https://doi.org/10.1016/S0040-4039(98)01426-9
TI - Bilane synthesis through bilene-a: An alternative approach
T2 - Tetrahedron Letters
AU - Xue, Tianhan
AU - Alan J. Scott, Alan
PY - 1998
DA - 1998/09/01
PB - Elsevier
SP - 6651-6654
IS - 37
VL - 39
SN - 0040-4039
SN - 1873-3581
ER -
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@article{1998_Xue,
author = {Tianhan Xue and Alan Alan J. Scott},
title = {Bilane synthesis through bilene-a: An alternative approach},
journal = {Tetrahedron Letters},
year = {1998},
volume = {39},
publisher = {Elsevier},
month = {sep},
url = {https://doi.org/10.1016/S0040-4039(98)01426-9},
number = {37},
pages = {6651--6654},
doi = {10.1016/S0040-4039(98)01426-9}
}
MLA
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Xue, Tianhan, et al. “Bilane synthesis through bilene-a: An alternative approach.” Tetrahedron Letters, vol. 39, no. 37, Sep. 1998, pp. 6651-6654. https://doi.org/10.1016/S0040-4039(98)01426-9.