ChemInform Abstract: Highly trans‐Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ‐Deoxygenation and Heck—Matsuda Reaction: Asymmetric Total Synthesis of (‐)‐Musellarins A—C (I) and Their Analogues. Issue 49 (December 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Highly trans‐Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ‐Deoxygenation and Heck—Matsuda Reaction: Asymmetric Total Synthesis of (‐)‐Musellarins A—C (I) and Their Analogues. Issue 49 (December 2015)
Main Title:: ChemInform Abstract: Highly trans‐Selective Arylation of Achmatowicz Rearrangement Products by Reductive γ‐Deoxygenation and Heck—Matsuda Reaction: Asymmetric Total Synthesis of (‐)‐Musellarins A—C (I) and Their Analogues.
Authors:: Li, Zhilong
Ip, Fanny C. F.
Ip, Nancy Y.
Tong, Rongbiao
Abstract:
Is Part Of:: ChemInform. Volume 46:Issue 49(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 49(2015)
Issue Display:: Volume 46, Issue 49 (2015)
Year:: 2015
Volume:: 46
Issue:: 49
Issue Sort Value:: 2015-0046-0049-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-12
Subjects:: other bioactive products
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.201549201 ↗
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:: 53.xml