77182-65-1

Usage

Uses

Used in Organic Synthesis:
(2S)-3β-Chloro-3,4,7,8-tetrahydro-2-[(E)-2-penten-4-ynyl]-8β-[(E)-1-propenyl]-2H-oxocin is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique functional groups facilitate multiple types of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Drug Development:
In the pharmaceutical industry, (2S)-3β-Chloro-3,4,7,8-tetrahydro-2-[(E)-2-penten-4-ynyl]-8β-[(E)-1-propenyl]-2H-oxocin is employed as a starting material for the development of new drugs. Its structural features may offer novel mechanisms of action or improved pharmacokinetic properties, contributing to the discovery of innovative therapeutic agents.
Used in Chemical Research:
(2S)-3β-Chloro-3,4,7,8-tetrahydro-2-[(E)-2-penten-4-ynyl]-8β-[(E)-1-propenyl]-2H-oxocin serves as a subject of study in chemical research, where its reactivity and the behavior of its functional groups are investigated. Understanding these aspects can lead to advancements in synthetic methodologies and the design of new chemical processes.
Used in Material Science:
In material science, (2S)-3β-Chloro-3,4,7,8-tetrahydro-2-[(E)-2-penten-4-ynyl]-8β-[(E)-1-propenyl]-2H-oxocin may be explored for its potential to contribute to the development of new materials with unique properties. Its structural components could be harnessed to create materials with specific applications in areas such as electronics, coatings, or advanced composites.

InChI:InChI=1/C15H19ClO/c1-3-5-6-12-15-14(16)11-8-7-10-13(17-15)9-4-2/h1,4-9,13-15H,10-12H2,2H3/b6-5+,8-7-,9-4+/t13-,14?,15?/m1/s1

Upstream product

• 477198-73-5 (2R,5R,8R)-5-(tert-butyldimethylsilyloxy)-8-[(1E)-propenyl]-2-[(2E)-5-trimethylsilylpent-2-en-4-ynyl]-oxocan-3-one 
• 477198-72-4 (2R,5R,8R)-5-(tert-butyldimethylsilyloxy)-8-(4-methoxyphenylmethoxymethyl)-2-[(2E)-5-trimethylsilylpent-2-en-4-ynyl]-oxocan-3-one 
• 477198-71-3 (2R,3S,5R,8R)-5-(tert-butyldimethylsilyloxy)-8-(4-methoxyphenylmethoxymethyl)-2-[(2E)-5-trimethylsilylpent-2-en-4-ynyl]-oxocan-3-ol 

Relevant academic research and scientific papers

Synthetic and Mechanistic Studies of the Retro-Claisen Rearrangement 4. An Application to the Total Synthesis of (+)-Laurenyne

(Matrix Presented) A novel asymmetric total synthesis of marine natural product (+)-Laurenyne has been achieved. The key elements of the strategy are the sequential metal ion-templated SN2′ cyclization affording a highly functionalized chiral vinyl cyclobutane and a retro-Claisen rearrangement for the construction of an eight-membered ring ether.