Highly Enantioselective Intramolecular Morita‐Baylis‐Hillman Reaction Catalyzed by Mannose‐Based Thiourea‐phosphine. Issue 10 (29th September 2015)
- Record Type:
- Journal Article
- Title:
- Highly Enantioselective Intramolecular Morita‐Baylis‐Hillman Reaction Catalyzed by Mannose‐Based Thiourea‐phosphine. Issue 10 (29th September 2015)
- Main Title:
- Highly Enantioselective Intramolecular Morita‐Baylis‐Hillman Reaction Catalyzed by Mannose‐Based Thiourea‐phosphine
- Authors:
- Yang, Weihong
Yuan, Kui
Song, Hongliang
Sha, Feng
Wu, Xinyan - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The saccharide‐based chiral bifunctional thiourea‐phosphines were developed as chiral organocatalysts for the intramolecular Morita‐Baylis‐Hillman reaction of <italic>ω</italic>‐formyl‐enones. With only 2 mol% of thiourea‐phosphine catalyst <bold>3c</bold>, chiral functionalized cyclohexenes were achieved under mild reaction conditions with excellent yields and enantioselectivities.</p> </abstract>
- Is Part Of:
- Chinese journal of chemistry. Volume 33:Issue 10(2015:Oct.)
- Journal:
- Chinese journal of chemistry
- Issue:
- Volume 33:Issue 10(2015:Oct.)
- Issue Display:
- Volume 33, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 33
- Issue:
- 10
- Issue Sort Value:
- 2015-0033-0010-0000
- Page Start:
- 1111
- Page End:
- 1114
- Publication Date:
- 2015-09-29
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1614-7065 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cjoc.201500468 ↗
- Languages:
- English
- ISSNs:
- 1001-604X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3180.299500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3137.xml