Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.

A. I. Meyers; Nicholas R. Natale; David G. Wettlaufer; Shahin Rafii; Jon Clardy

doi:10.1016/S0040-4039(01)92436-0

Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.

A. I. Meyers
, Nicholas R. Natale
, David G. Wettlaufer
, Shahin Rafii
, Jon Clardy

Research output: Contribution to journal › Article › peer-review

54 Scopus citations

Abstract

Addition of organometallics to chiral 3-pyridyl oxazolines gave high diastereoselectivity at the 4-position of the pyridine nucleus. Absolute configuration was determined by x-ray analysis.

Original language	English
Pages (from-to)	5123-5126
Number of pages	4
Journal	Tetrahedron Letters
Volume	22
Issue number	51
DOIs	https://doi.org/10.1016/S0040-4039(01)92436-0
State	Published - 1981

Funding

The authors thank the National Science Foundation

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10.1016/S0040-4039(01)92436-0

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@article{d8bc74ec3a3f42f1b6d94e835b65e27c,

title = "Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.",

abstract = "Addition of organometallics to chiral 3-pyridyl oxazolines gave high diastereoselectivity at the 4-position of the pyridine nucleus. Absolute configuration was determined by x-ray analysis.",

author = "Meyers, \{A. I.\} and Natale, \{Nicholas R.\} and Wettlaufer, \{David G.\} and Shahin Rafii and Jon Clardy",

note = "Funding Information: The authors thank the National Science Foundation",

year = "1981",

doi = "10.1016/S0040-4039(01)92436-0",

language = "English",

volume = "22",

pages = "5123--5126",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "51",

}

TY - JOUR

T1 - Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.

AU - Meyers, A. I.

AU - Natale, Nicholas R.

AU - Wettlaufer, David G.

AU - Rafii, Shahin

AU - Clardy, Jon

N1 - Funding Information: The authors thank the National Science Foundation

PY - 1981

Y1 - 1981

N2 - Addition of organometallics to chiral 3-pyridyl oxazolines gave high diastereoselectivity at the 4-position of the pyridine nucleus. Absolute configuration was determined by x-ray analysis.

AB - Addition of organometallics to chiral 3-pyridyl oxazolines gave high diastereoselectivity at the 4-position of the pyridine nucleus. Absolute configuration was determined by x-ray analysis.

UR - https://www.scopus.com/pages/publications/0000769051

U2 - 10.1016/S0040-4039(01)92436-0

DO - 10.1016/S0040-4039(01)92436-0

M3 - Article

AN - SCOPUS:0000769051

SN - 0040-4039

VL - 22

SP - 5123

EP - 5126

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 51

ER -

Chiral 1,4-dihydropyridines. Synthesis and absolute configuration.

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