Related references
Note: Only part of the references are listed.New Insights into the Chemical Composition, Pro-Inflammatory Cytokine Inhibition Profile of Davana (Artemisia pallens Wall. ex DC.) Essential Oil and cis-Davanone in Primary Macrophage Cells
Swati Singh et al.
CHEMISTRY & BIODIVERSITY (2021)
Diversity-Oriented Approach to N-Heterocyclic Compounds from alpha-Phenyl-beta-enamino Ester via a Mitsunobu-Michael Reaction Sequence
Hina P. A. Khan et al.
JOURNAL OF ORGANIC CHEMISTRY (2018)
Direct, Biomimetic Synthesis of (+)-Artemone via a Stereoselective, Organocatalytic Cyclization
Eric D. Nacsa et al.
SYNTHESIS-STUTTGART (2015)
Synthesis and olfactory properties of unnatural derivatives of lilac aldehydes
Peter Siska et al.
TETRAHEDRON (2014)
Synthesis of cis- and trans-Davanoids: Artemone, Hydroxydavanone, Isodavanone, and Nordavanone
Kanny K. Wan et al.
SYNTHESIS-STUTTGART (2013)
Efforts toward rapid construction of the cortistatin A carbocyclic core via enyne-ene metathesis
Corinne Baumgartner et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2010)
Stereospecific Total Synthesis of (+)-Davana Acid, (+)-Nordavanone and (+)-Davanone
Gowravaram Sabitha et al.
SYNTHESIS-STUTTGART (2010)
A Concise, Biomimetic Total Synthesis of (+)-Davanone
Karen C. Morrison et al.
ORGANIC LETTERS (2009)
Stereospecific debenzylative cycloetherification of carbohydrate-derived allylic alcohols, ethers and esters to form vinyl C-furanosides
Riccardo Cribiu et al.
CHEMICAL COMMUNICATIONS (2008)
Antifungal activity of davanone-type sesquiterpenes from Artemisia lobelii var. conescens
V Vajs et al.
JOURNAL OF THE SERBIAN CHEMICAL SOCIETY (2004)
Stereochemical disposition of the geminal dimethyl groups in the enzymatic cyclization of geranyl diphosphate to (+)-bornyl diphosphate by recombinant (+)-bornyl diphosphate synthase from Salvia officinalis
ML Wise et al.
TETRAHEDRON (2001)
Titanium enolates of thiazolidinethione chiral auxiliaries: Versatile tools for asymmetric aldol additions
MT Crimmins et al.
ORGANIC LETTERS (2000)
Share Paper
