Asymmetric synthesis of 2,4-disubstituted pyrrolidines
1
Institut de chimie des substances naturelles, CNRS 91198-Gif-sur-Yvette, France
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Publication type: Journal Article
Publication date: 1998-08-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
A new strategy for asymmetric synthesis of 2,4-disubstituted pyrrolidines is described, starting from readily available chiral building blocks 1 and (2 R )-2,3- O -isopropylideneglycealdehyde ( 6 ). An efficient synthesis of enentiomerically pure compounds 2 and 3 was developed starting from chiral synthon 1
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Wang Q., Sasaki N., Potier P. Asymmetric synthesis of 2,4-disubstituted pyrrolidines // Tetrahedron Letters. 1998. Vol. 39. No. 32. pp. 5755-5758.
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Wang Q., Sasaki N., Potier P. Asymmetric synthesis of 2,4-disubstituted pyrrolidines // Tetrahedron Letters. 1998. Vol. 39. No. 32. pp. 5755-5758.
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RIS
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TY - JOUR
DO - 10.1016/s0040-4039(98)01171-x
UR - https://doi.org/10.1016/s0040-4039(98)01171-x
TI - Asymmetric synthesis of 2,4-disubstituted pyrrolidines
T2 - Tetrahedron Letters
AU - Wang, Qian
AU - Sasaki, N.André
AU - Potier, Pierre
PY - 1998
DA - 1998/08/01
PB - Elsevier
SP - 5755-5758
IS - 32
VL - 39
SN - 0040-4039
SN - 1873-3581
ER -
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BibTex (up to 50 authors)
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@article{1998_Wang,
author = {Qian Wang and N.André Sasaki and Pierre Potier},
title = {Asymmetric synthesis of 2,4-disubstituted pyrrolidines},
journal = {Tetrahedron Letters},
year = {1998},
volume = {39},
publisher = {Elsevier},
month = {aug},
url = {https://doi.org/10.1016/s0040-4039(98)01171-x},
number = {32},
pages = {5755--5758},
doi = {10.1016/s0040-4039(98)01171-x}
}
Cite this
MLA
Copy
Wang, Qian, et al. “Asymmetric synthesis of 2,4-disubstituted pyrrolidines.” Tetrahedron Letters, vol. 39, no. 32, Aug. 1998, pp. 5755-5758. https://doi.org/10.1016/s0040-4039(98)01171-x.