Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a C-13 NMR chemical shift/structure correlation.

Saved in:
Bibliographic Details
Published inOrganic & biomolecular chemistry Vol. 7; no. 2; pp. 238 - 252
Main Authors Sheldrake, Helen M., Jamieson, Craig, Pascu, Sofia I., Burton, Jonathan W.
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 01.01.2009
Subjects
Alkenes - chemical synthesis
Alkenes - chemistry
Alkynes - chemical synthesis
Alkynes - chemistry
Biological Products - chemical synthesis
Chemistry
Chemistry, Organic
Furans - chemical synthesis
Furans - chemistry
Laurencia - chemistry
Magnetic Resonance Spectroscopy
Physical Sciences
Science & Technology
Stereoisomerism
SUPRAMOLECULAR HOST SYSTEMS
ALLYLIC ALCOHOLS
KEY INTERMEDIATE
C-GLYCOSIDES
STEREOSELECTIVE-SYNTHESIS
EMPLOYING CELLOBIOSE
STEREOCONTROLLED SYNTHESIS
POLYCYCLIC ETHERS
2-DIRECTIONAL CHAIN SYNTHESIS
MARINE NATURAL-PRODUCTS
Online AccessGet full text

Cover

More Information
Summary:A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a C-13 NMR chemical shift/structure correlation.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1477-0520
1477-0539
DOI:10.1039/b814953d