ChemInform Abstract: Stereoselective Synthesis of (Sulfonimidoyl)cyclopropanes with (R)‐PhSO(NTs)CH2Cl and α, β‐Unsaturated Weinreb Amides: Tuning the of Selectivity Between C—Cl and C—S Bond Cleavage. Issue 27 (16th June 2016)

Record Type:: Journal Article
Title:: ChemInform Abstract: Stereoselective Synthesis of (Sulfonimidoyl)cyclopropanes with (R)‐PhSO(NTs)CH2Cl and α, β‐Unsaturated Weinreb Amides: Tuning the of Selectivity Between C—Cl and C—S Bond Cleavage. Issue 27 (16th June 2016)
Main Title:: ChemInform Abstract: Stereoselective Synthesis of (Sulfonimidoyl)cyclopropanes with (R)‐PhSO(NTs)CH2Cl and α, β‐Unsaturated Weinreb Amides: Tuning the of Selectivity Between C—Cl and C—S Bond Cleavage.
Authors:: Shen, Xiao
Liu, Qinghe
Zhang, Wei
Hu, Jinbo
Abstract:: Abstract: The Weinreb amide group and the counter cation of the base are important for the selective C‐Cl bond cleavage of (R)‐PhSO(NTs)CH2 Cl.
Is Part Of:: ChemInform. Volume 47:Issue 27(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 27(2016)
Issue Display:: Volume 47, Issue 27 (2016)
Year:: 2016
Volume:: 47
Issue:: 27
Issue Sort Value:: 2016-0047-0027-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-06-16
Subjects:: cyclopropane derivatives -- cyclopropanation reactions -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201627075 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 454.xml