Organocatalytic synthesis of multiple substituted b[4.4.0]decalin system

Shaik Anwar; Hui Ju Chang; Kwunmin Chen

doi:10.1021/ol200424x

Organocatalytic synthesis of multiple substituted b[4.4.0]decalin system

Shaik Anwar, Hui Ju Chang, Kwunmin Chen^*

^*Corresponding author for this work

Department of Chemistry

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

43 Citations (Scopus)

Abstract

Chemical equations presented. An efficient and unprecedented organocatalytic reaction of γ-nitroketones with α,β-unsaturated aldehydes to give polyfunctionalized [4.4.0] bicyclic skeletons was developed. The diphenylprolinol silyl ether mediated nitro-Michael/Aldol reaction afforded the hexa-substituted decalin carboaldehydes with excellent diastereo- and enantioselectivity (up to >99:1 dr and >99% ee) via a formal [4 + 2] carbocyclization process.

Original language	English
Pages (from-to)	2200-2203
Number of pages	4
Journal	Organic Letters
Volume	13
Issue number	9
DOIs	https://doi.org/10.1021/ol200424x
Publication status	Published - 2011 May 6

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol200424x

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title = "Organocatalytic synthesis of multiple substituted b[4.4.0]decalin system",

abstract = "Chemical equations presented. An efficient and unprecedented organocatalytic reaction of γ-nitroketones with α,β-unsaturated aldehydes to give polyfunctionalized [4.4.0] bicyclic skeletons was developed. The diphenylprolinol silyl ether mediated nitro-Michael/Aldol reaction afforded the hexa-substituted decalin carboaldehydes with excellent diastereo- and enantioselectivity (up to >99:1 dr and >99% ee) via a formal [4 + 2] carbocyclization process.",

author = "Shaik Anwar and Chang, {Hui Ju} and Kwunmin Chen",

year = "2011",

month = may,

day = "6",

doi = "10.1021/ol200424x",

language = "English",

volume = "13",

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journal = "Organic Letters",

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AU - Anwar, Shaik

AU - Chang, Hui Ju

AU - Chen, Kwunmin

PY - 2011/5/6

Y1 - 2011/5/6

N2 - Chemical equations presented. An efficient and unprecedented organocatalytic reaction of γ-nitroketones with α,β-unsaturated aldehydes to give polyfunctionalized [4.4.0] bicyclic skeletons was developed. The diphenylprolinol silyl ether mediated nitro-Michael/Aldol reaction afforded the hexa-substituted decalin carboaldehydes with excellent diastereo- and enantioselectivity (up to >99:1 dr and >99% ee) via a formal [4 + 2] carbocyclization process.

AB - Chemical equations presented. An efficient and unprecedented organocatalytic reaction of γ-nitroketones with α,β-unsaturated aldehydes to give polyfunctionalized [4.4.0] bicyclic skeletons was developed. The diphenylprolinol silyl ether mediated nitro-Michael/Aldol reaction afforded the hexa-substituted decalin carboaldehydes with excellent diastereo- and enantioselectivity (up to >99:1 dr and >99% ee) via a formal [4 + 2] carbocyclization process.

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JO - Organic Letters

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Organocatalytic synthesis of multiple substituted b[4.4.0]decalin system

Abstract

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CCDC 805805: Experimental Crystal Structure Determination

CCDC 806842: Experimental Crystal Structure Determination

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Organocatalytic synthesis of multiple substituted b[4.4.0]decalin system

Abstract

ASJC Scopus subject areas

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Datasets

CCDC 805805: Experimental Crystal Structure Determination

CCDC 806842: Experimental Crystal Structure Determination

Cite this