Preparation of Bicyclo[4.3.0.]nonanes by an Organocatalytic Intramolecular Diels-Alder Reaction

Ari M.P. Koskinen; Sami A. Selkälä

doi:10.1002/ejoc.200400802

Preparation of Bicyclo[4.3.0.]nonanes by an Organocatalytic Intramolecular Diels-Alder Reaction

Ari M.P. Koskinen
, Sami A. Selkälä

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

44 Citations (Scopus)

547 Downloads (Pure)

Abstract

The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A novel enantioselective organocatalytic cycloaddition was used to prepare the bicyclo[4.3.0]nonane skeleton.

Original language	English
Pages (from-to)	1620-1624
Journal	European Journal of Organic Chemistry
DOIs	https://doi.org/10.1002/ejoc.200400802
Publication status	Published - 2005
MoE publication type	A1 Journal article-refereed

Keywords

cucloaddition
enantioselectivity
natural products
organocatalysis

Access to Document

10.1002/ejoc.200400802

ms112Accepted author manuscript, 88.9 KB

Cite this

@article{b23cb450a8fa407897a08a02bf896188,

title = "Preparation of Bicyclo[4.3.0.]nonanes by an Organocatalytic Intramolecular Diels-Alder Reaction",

abstract = "The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A novel enantioselective organocatalytic cycloaddition was used to prepare the bicyclo[4.3.0]nonane skeleton.",

keywords = "cucloaddition, enantioselectivity, natural products, organocatalysis, cucloaddition, enantioselectivity, natural products, organocatalysis, cucloaddition, enantioselectivity, natural products, organocatalysis",

author = "Koskinen, \{Ari M.P.\} and Selk{\"a}l{\"a}, \{Sami A.\}",

year = "2005",

doi = "10.1002/ejoc.200400802",

language = "English",

pages = "1620--1624",

journal = "European Journal of Organic Chemistry",

issn = "1099-0690",

publisher = "Wiley",

}

TY - JOUR

T1 - Preparation of Bicyclo[4.3.0.]nonanes by an Organocatalytic Intramolecular Diels-Alder Reaction

AU - Koskinen, Ari M.P.

AU - Selkälä, Sami A.

PY - 2005

Y1 - 2005

N2 - The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A novel enantioselective organocatalytic cycloaddition was used to prepare the bicyclo[4.3.0]nonane skeleton.

AB - The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A novel enantioselective organocatalytic cycloaddition was used to prepare the bicyclo[4.3.0]nonane skeleton.

KW - cucloaddition

KW - enantioselectivity

KW - natural products

KW - organocatalysis

KW - cucloaddition

KW - enantioselectivity

KW - natural products

KW - organocatalysis

KW - cucloaddition

KW - enantioselectivity

KW - natural products

KW - organocatalysis

U2 - 10.1002/ejoc.200400802

DO - 10.1002/ejoc.200400802

M3 - Article

SN - 1099-0690

SP - 1620

EP - 1624

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

ER -

Preparation of Bicyclo[4.3.0.]nonanes by an Organocatalytic Intramolecular Diels-Alder Reaction

Abstract

Keywords

Access to Document

Fingerprint

Cite this