Enantioselective methodologies for the synthesis of spiro compounds
Тип публикации: Journal Article
Дата публикации: 2012-01-01
scimago Q1
wos Q1
БС1
SJR: 11.467
CiteScore: 73.2
Impact factor: 39
ISSN: 03060012, 14604744
PubMed ID:
21975423
General Chemistry
Краткое описание
The enantioselective synthesis of spirocycles has been a long time pursued dream for organic chemists. Since the first pioneering efforts of Tamao and coworkers in the enantioselective construction of spirosilanes, many efforts have been devoted to the development of new and promising asymmetric methodologies. Remarkably, with the advent of organocatalysis the number of methodologies has been highly increased. The aim of this tutorial review is to summarize the last trends and developments reported in the literature in the enantioselective synthesis of spirocompounds.
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ГОСТ
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Rios R. Enantioselective methodologies for the synthesis of spiro compounds // Chemical Society Reviews. 2012. Vol. 41. No. 3. pp. 1060-1074.
ГОСТ со всеми авторами (до 50)
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Rios R. Enantioselective methodologies for the synthesis of spiro compounds // Chemical Society Reviews. 2012. Vol. 41. No. 3. pp. 1060-1074.
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RIS
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TY - JOUR
DO - 10.1039/C1CS15156H
UR - https://doi.org/10.1039/C1CS15156H
TI - Enantioselective methodologies for the synthesis of spiro compounds
T2 - Chemical Society Reviews
AU - Rios, Ramon
PY - 2012
DA - 2012/01/01
PB - Royal Society of Chemistry (RSC)
SP - 1060-1074
IS - 3
VL - 41
PMID - 21975423
SN - 0306-0012
SN - 1460-4744
ER -
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BibTex (до 50 авторов)
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@article{2012_Rios,
author = {Ramon Rios},
title = {Enantioselective methodologies for the synthesis of spiro compounds},
journal = {Chemical Society Reviews},
year = {2012},
volume = {41},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/C1CS15156H},
number = {3},
pages = {1060--1074},
doi = {10.1039/C1CS15156H}
}
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MLA
Скопировать
Rios, Ramon. “Enantioselective methodologies for the synthesis of spiro compounds.” Chemical Society Reviews, vol. 41, no. 3, Jan. 2012, pp. 1060-1074. https://doi.org/10.1039/C1CS15156H.