214282-99-2

Upstream product

• 4463-33-6 1,2-dimethoxy-3-methylbenzene 

Downstream Products

• 214283-02-0 ethyl (E,4S)-4-[(2,3-dimethoxy-4-methyl)phenyl]pent-2-enoate 
• 75889-47-3 2,3-dimethoxy-4-methylbenzaldehyde 
• 1284222-78-1 (S)-1-(but-3-en-2-yl)-2,3-dimethoxy-4-methylbenzene 
• 1284222-79-2 (S)-1-(4-iodobutan-2-yl)-2,3-dimethoxy-4-methylbenzene 
• 1284222-88-3 (S)-3-(2,3-dimethoxy-4-methylphenyl)butan-1-ol 
• 951161-56-1 2,3-dimethoxy-1-methyl-4-vinylbenzene 
• 214283-09-7 (1S,4S)-1-((R)-3-Benzenesulfonyl-1,5-dimethyl-hex-4-enyl)-5,6-dimethoxy-4,7-dimethyl-1,2,3,4-tetrahydro-naphthalene 
• 214283-08-6 Toluene-4-sulfonic acid (S)-2-((1S,4S)-5,6-dimethoxy-4,7-dimethyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-propyl ester 
• 214283-03-1 (S)-4-(2,3-dimethoxy-4-methylphenyl)pentanal 
• 406672-93-3 (3RS,6R)-6-(2,3-dimethoxy-4-methylphenyl)-1-trimethylsilylhept-1-yn-3-ol 
• 406672-92-2 (R)-4-(2,3-dimethoxy-4-methylphenyl)pentanal 
• 214283-04-2 (3RS,6S)-6-(2,3-dimethoxy-4-methylphenyl)-1-trimethylsilylhept-1-yn-3-ol 

Relevant academic research and scientific papers

Broadly Applicable Stereoselective Syntheses of Serrulatane, Amphilectane Diterpenes, and Their Diastereoisomeric Congeners Using Asymmetric Hydrovinylation for Absolute Stereochemical Control

A stereogenic center, placed at an exocyclic location next to a chiral carbon in a ring to which it is attached, is a ubiquitous structural motif seen in many bioactive natural products, including di- and triterpenes and steroids. Installation of these ce

Enantiospecific syntheses of pseudopterosin aglycones - Part 1. Synthesis of the putative aglycone of pseudopterosin G-J via an A→AB→ABC annulation strategy

The putative aglycone of pseudopterosin G-J and its enantiomer were synthesised enantiospecifically from 2,3-dimethoxytoluene and η3-allyl cationic complexes of molybdenum and iron respectively. The A→AB→ABC annulation strategy entailed the use of allyl cations or their equivalents for the creation of the three benzylic stereogenic centres. The X-ray structure of tetrahydronaphthalene (-)-41a was determined.