One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction

Hao Li; Jian Wang; Timiyin E-Nunu; Liansuo Zu; Wei Jiang; Shaohua Wei; Wei Wang

doi:10.1039/b611502k

One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction

Hao Li, Jian Wang, Timiyin E-Nunu, Liansuo Zu, Wei Jiang, Shaohua Wei, Wei Wang

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

164 Scopus citations

Abstract

A highly enantioselective (S)-diphenylpyrrolinol triethylsilyl ether promoted tandem oxa-Michael-aldol reaction of α,β-unsaturated aldehydes with salicylaldehydes has been developed; the method affords one-pot access to chiral and synthetically useful chromenes in high yields and high enantioselectivities from readily available compounds.

Original language	English (US)
Pages (from-to)	507-509
Number of pages	3
Journal	Chemical Communications
Issue number	5
DOIs	https://doi.org/10.1039/b611502k
State	Published - 2007
Externally published	Yes

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
General Chemistry
Ceramics and Composites
Metals and Alloys
Materials Chemistry
Surfaces, Coatings and Films
Catalysis

Access to Document

10.1039/b611502k

Cite this

@article{732a5ab78b854650a6b353e3fa1739b0,

title = "One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction",

abstract = "A highly enantioselective (S)-diphenylpyrrolinol triethylsilyl ether promoted tandem oxa-Michael-aldol reaction of α,β-unsaturated aldehydes with salicylaldehydes has been developed; the method affords one-pot access to chiral and synthetically useful chromenes in high yields and high enantioselectivities from readily available compounds.",

author = "Hao Li and Jian Wang and Timiyin E-Nunu and Liansuo Zu and Wei Jiang and Shaohua Wei and Wei Wang",

year = "2007",

doi = "10.1039/b611502k",

language = "English (US)",

pages = "507--509",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "5",

}

TY - JOUR

T1 - One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction

AU - Li, Hao

AU - Wang, Jian

AU - E-Nunu, Timiyin

AU - Zu, Liansuo

AU - Jiang, Wei

AU - Wei, Shaohua

AU - Wang, Wei

PY - 2007

Y1 - 2007

N2 - A highly enantioselective (S)-diphenylpyrrolinol triethylsilyl ether promoted tandem oxa-Michael-aldol reaction of α,β-unsaturated aldehydes with salicylaldehydes has been developed; the method affords one-pot access to chiral and synthetically useful chromenes in high yields and high enantioselectivities from readily available compounds.

AB - A highly enantioselective (S)-diphenylpyrrolinol triethylsilyl ether promoted tandem oxa-Michael-aldol reaction of α,β-unsaturated aldehydes with salicylaldehydes has been developed; the method affords one-pot access to chiral and synthetically useful chromenes in high yields and high enantioselectivities from readily available compounds.

UR - https://www.scopus.com/pages/publications/33846528479

UR - https://www.scopus.com/inward/citedby.url?scp=33846528479&partnerID=8YFLogxK

U2 - 10.1039/b611502k

DO - 10.1039/b611502k

M3 - Article

C2 - 17252110

AN - SCOPUS:33846528479

SN - 1359-7345

SP - 507

EP - 509

JO - Chemical Communications

JF - Chemical Communications

IS - 5

ER -

One-pot approach to chiral chromenes via enantioselective organocatalytic domino oxa-Michael-aldol reaction

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this