Asymmetric synthesis of (+)-trans-aerangis lactone

Aejin Kim; Satyasheel Sharma; Jong Hwan Kwak; In Su Kim

doi:10.5012/bkcs.2013.34.1.75

Asymmetric synthesis of (+)-trans-aerangis lactone

Aejin Kim, Satyasheel Sharma, Jong Hwan Kwak, In Su Kim

Department of Pharmacy

Sungkyunkwan University

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

6 Scopus citations

Abstract

Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis.

Original language	English
Pages (from-to)	75-78
Number of pages	4
Journal	Bulletin of the Korean Chemical Society
Volume	34
Issue number	1
DOIs	https://doi.org/10.5012/bkcs.2013.34.1.75
State	Published - 20 Jan 2013

Keywords

Aerangis lactone
Asymmetric
Catalytic
Crotylation
Metathesis

Access to Document

10.5012/bkcs.2013.34.1.75

Cite this

@article{21c852d5d62b449b848f8f5f857d38d2,

title = "Asymmetric synthesis of (+)-trans-aerangis lactone",

abstract = "Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis.",

keywords = "Aerangis lactone, Asymmetric, Catalytic, Crotylation, Metathesis",

author = "Aejin Kim and Satyasheel Sharma and Kwak, \{Jong Hwan\} and Kim, \{In Su\}",

year = "2013",

month = jan,

day = "20",

doi = "10.5012/bkcs.2013.34.1.75",

language = "English",

volume = "34",

pages = "75--78",

journal = "Bulletin of the Korean Chemical Society",

issn = "0253-2964",

publisher = "Wiley-Blackwell",

number = "1",

}

TY - JOUR

T1 - Asymmetric synthesis of (+)-trans-aerangis lactone

AU - Kim, Aejin

AU - Sharma, Satyasheel

AU - Kwak, Jong Hwan

AU - Kim, In Su

PY - 2013/1/20

Y1 - 2013/1/20

N2 - Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis.

AB - Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis.

KW - Aerangis lactone

KW - Asymmetric

KW - Catalytic

KW - Crotylation

KW - Metathesis

UR - https://www.scopus.com/pages/publications/84872960971

U2 - 10.5012/bkcs.2013.34.1.75

DO - 10.5012/bkcs.2013.34.1.75

M3 - Article

AN - SCOPUS:84872960971

SN - 0253-2964

VL - 34

SP - 75

EP - 78

JO - Bulletin of the Korean Chemical Society

JF - Bulletin of the Korean Chemical Society

IS - 1

ER -

Asymmetric synthesis of (+)-trans-aerangis lactone

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this