Similar Papers

Paper Title
Journal
Date
Author
A two-step synthesis of allylic syn 1,3-diols via an intramolecular oxa-Michael reaction followed by a modified Julia olefination
Raphaël Oriez ... Joëlle Prunet
Tetrahedron Letters | VOL. 51
Raphaël Oriez, et. al.Raphaël Oriez ... Joëlle Prunet
03 Nov 2009
Synthesis of Modified Methyl Furanosides by Intramolecular Oxa-Michael Reaction followed by Pummerer Rearrangement
Diego Gamba-Sanchez ... Joëlle Prunet
The Journal of Organic Chemistry | VOL. 75
Diego Gamba-Sanchez, et. al.Diego Gamba-Sanchez ... Joëlle Prunet
12 Apr 2010
Synthesis of Sultam Scaffolds via Intramolecular Oxa-Michael and Diastereoselective Baylis−Hillman Reactions
Aihua Zhou ... Paul R Hanson
Organic Letters | VOL. 10
Aihua Zhou, et. al.Aihua Zhou ... Paul R Hanson
14 Jun 2008
Asymmetric synthesis of (+)-passifloricin A and its 6-epimer
S Chandrasekhar ... A Syamprasad Reddy
Tetrahedron Letters | VOL. 49
S Chandrasekhar, et. al.S Chandrasekhar ... A Syamprasad Reddy
16 May 2008
View more papers

More From: HETEROCYCLES

Paper Title
Journal
Date
Author
Contents
Heterocycles Contents
HETEROCYCLES | VOL. 106
Heterocycles ContentsHeterocycles Contents
01 Jan 2023
Contents
Heterocycles Contents
HETEROCYCLES | VOL. 106
Heterocycles ContentsHeterocycles Contents
01 Jan 2023
New C19-Diterpeniod Alkaloids from Aconitum novoluridum
Xianli Zhou ... Yan Xiao
HETEROCYCLES | VOL. 106
Xianli Zhou, et. al.Xianli Zhou ... Yan Xiao
01 Jan 2023
Hydroxychloroquine: Chemistry and Medicinal Applications
Ram Singh ... Nidhi Yadav
HETEROCYCLES | VOL. 106
Ram Singh, et. al.Ram Singh ... Nidhi Yadav
01 Jan 2023
View more papers

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.