ChemInform Abstract: The Synthesis of the δ‐Lactone Portion of the Mevinic Acids. A New Non‐Acidic Method of Cyclic Lactone Expansion.

A H Davidson,P L Myers,C D Floyd,C N Lewis

doi:10.1002/chin.198919196

ChemInform Abstract: The Synthesis of the δ‐Lactone Portion of the Mevinic Acids. A New Non‐Acidic Method of Cyclic Lactone Expansion.

A H Davidson, P L Myers + Show 2 more

https://doi.org/10.1002/chin.198919196

Copy DOI

Export

Save

Cite

Journal: ChemInform

Publication Date: May 9, 1989

Affiliation: Cardiff University

#Chiral Lactone #Cyclic Expansion #Vinylic Sulfide #Method Of Expansion #Mevinic Acids #Cyclic Lactone #Phenyl Sulfide

Abstract
Full-Text
Similar Papers

Abstract

Listen

AbstractThe readily available chiral lactone (I) is transformed into the vinylic phenyl sulfide (II) which is cyclized upon methoxymercuration and reduction, producing the tetrahydropyran (IV).

Full Text

Published Version

Check institute access

Open DOI Link

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Similar Papers

Paper Title

Journal

Date

Author

View more papers

More From: ChemInform

Paper Title

Journal

Date

Author

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.

R Discovery Prime

ChemInform Abstract: The Synthesis of the δ‐Lactone Portion of the Mevinic Acids. A New Non‐Acidic Method of Cyclic Lactone Expansion.