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	Funder number
Japan Society for the Promotion

Access to Document

10.1080/00397910008087321

Cite this

@article{570a74315e0e4121878e5a941e01b618,

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",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

number = "2",

}

TY - JOUR

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.

UR - http://www.scopus.com/inward/record.url?scp=0033950585&partnerID=8YFLogxK

U2 - 10.1080/00397910008087321

DO - 10.1080/00397910008087321

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:0033950585

SN - 0039-7911

VL - 30

SP - 293

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

Bibliographical note

Funding

Access to Document

Other files and links

Fingerprint

Cite this