Stereoselective conjugate additions of alcohols to a chiral (E)- nitroalkene derived from (R)-2,3-isopropylidene glyceraldehyde

Qian Cheng; Takayuki Oritani; Alfred Hassner

doi:10.1080/00397910008087321

Stereoselective conjugate additions of alcohols to a chiral (E)- nitroalkene derived from (R)-2,3-isopropylidene glyceraldehyde

Qian Cheng
, Takayuki Oritani
, Alfred Hassner

Department of Chemistry

Tohoku University

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

6 Scopus citations

Abstract

Addition of functionalized alcohols to a chiral (E)-nitroalkene proceeded with modest to high diastereoselectivities depending on the presence of metal catalysts in low temperature. The results indicated that anti-selectivities were preferred in all cases.

Original language	English
Pages (from-to)	293-300
Number of pages	8
Journal	Synthetic Communications
Volume	30
Issue number	2
DOIs	https://doi.org/10.1080/00397910008087321
State	Published - 2000

Bibliographical note

Funding Information:
Financial support by Monbusho Grant-in-Aid from Japan Society for the Promotion

Funding

Financial support by Monbusho Grant-in-Aid from Japan Society for the Promotion

Funders
Japan Society for the Promotion

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10.1080/00397910008087321

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title = "Stereoselective conjugate additions of alcohols to a chiral (E)- nitroalkene derived from (R)-2,3-isopropylidene glyceraldehyde",

abstract = "Addition of functionalized alcohols to a chiral (E)-nitroalkene proceeded with modest to high diastereoselectivities depending on the presence of metal catalysts in low temperature. The results indicated that anti-selectivities were preferred in all cases.",

author = "Qian Cheng and Takayuki Oritani and Alfred Hassner",

note = "Funding Information: Financial support by Monbusho Grant-in-Aid from Japan Society for the Promotion",

year = "2000",

doi = "10.1080/00397910008087321",

language = "אנגלית",

volume = "30",

pages = "293--300",

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T1 - Stereoselective conjugate additions of alcohols to a chiral (E)- nitroalkene derived from (R)-2,3-isopropylidene glyceraldehyde

AU - Cheng, Qian

AU - Oritani, Takayuki

AU - Hassner, Alfred

N1 - Funding Information: Financial support by Monbusho Grant-in-Aid from Japan Society for the Promotion

PY - 2000

Y1 - 2000

N2 - Addition of functionalized alcohols to a chiral (E)-nitroalkene proceeded with modest to high diastereoselectivities depending on the presence of metal catalysts in low temperature. The results indicated that anti-selectivities were preferred in all cases.

AB - Addition of functionalized alcohols to a chiral (E)-nitroalkene proceeded with modest to high diastereoselectivities depending on the presence of metal catalysts in low temperature. The results indicated that anti-selectivities were preferred in all cases.

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DO - 10.1080/00397910008087321

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AN - SCOPUS:0033950585

SN - 0039-7911

VL - 30

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EP - 300

JO - Synthetic Communications

JF - Synthetic Communications

IS - 2

ER -

Stereoselective conjugate additions of alcohols to a chiral (E)- nitroalkene derived from (R)-2,3-isopropylidene glyceraldehyde

Abstract

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