Tetrahedron Letters, volume 39, issue 32, pages 5755-5758

Asymmetric synthesis of 2,4-disubstituted pyrrolidines

Qian Wang ¹

N.André Sasaki ¹

Pierre Potier ¹

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Institut de chimie des substances naturelles, CNRS 91198-Gif-sur-Yvette, France |

Publication type: Journal Article

Publication date: 1998-08-01

Elsevier

Journal: Tetrahedron Letters

scimago Q3

wos Q3

SJR: 0.323

CiteScore: 3.5

Impact factor: 1.5

ISSN: 00404039, 18733581

DOI: 10.1016/s0040-4039(98)01171-x

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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

Found

	1 2 3
Tetrahedron	Tetrahedron, 3, 30% Tetrahedron 3 publications, 30%
Tetrahedron Letters	Tetrahedron Letters, 1, 10% Tetrahedron Letters 1 publication, 10%
ChemistrySelect	ChemistrySelect, 1, 10% ChemistrySelect 1 publication, 10%
ChemInform	ChemInform, 1, 10% ChemInform 1 publication, 10%
Journal of Organic Chemistry	Journal of Organic Chemistry, 1, 10% Journal of Organic Chemistry 1 publication, 10%
	1 2 3

	1 2 3 4
Elsevier	Elsevier, 4, 40% Elsevier 4 publications, 40%
Wiley	Wiley, 2, 20% Wiley 2 publications, 20%
American Chemical Society (ACS)	American Chemical Society (ACS), 1, 10% American Chemical Society (ACS) 1 publication, 10%
	1 2 3 4

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Publisher

Elsevier

Journal

Tetrahedron Letters

scimago Q3

wos Q3

SJR

0.323

CiteScore

3.5

Impact factor

1.5

ISSN

00404039 (Print)

18733581 (Electronic)

Asymmetric synthesis of 2,4-disubstituted pyrrolidines

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