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Usage

Uses

Used in Organic Synthesis:
(3S)-Dihydro-3-[(tetrahydro-2H-pyran-2-yl)oxy]-2(3H)-furanone is used as a key intermediate in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows it to participate in a wide range of reactions, making it a versatile building block for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3S)-Dihydro-3-[(tetrahydro-2H-pyran-2-yl)oxy]-2(3H)-furanone is used as a starting material or intermediate in the synthesis of various drug candidates. Its ability to form stable derivatives and participate in multiple types of chemical reactions makes it an essential component in the development of new and innovative medications.
Used in Agrochemical Industry:
(3S)-Dihydro-3-[(tetrahydro-2H-pyran-2-yl)oxy]-2(3H)-furanone is also utilized in the agrochemical industry for the synthesis of various crop protection agents and pesticides. Its unique properties enable it to be incorporated into the development of new and effective products that help protect crops from pests and diseases.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, (3S)-Dihydro-3-[(tetrahydro-2H-pyran-2-yl)oxy]-2(3H)-furanone is used as a building block for the creation of unique and complex scents and flavors. Its ability to form stable derivatives and participate in various chemical reactions allows it to be used in the development of novel fragrances and flavor compounds.
Used in Research and Development:
(3S)-Dihydro-3-[(tetrahydro-2H-pyran-2-yl)oxy]-2(3H)-furanone is also used in research and development settings for the study of new chemical reactions and processes. Its unique structure and properties make it an ideal candidate for exploring new synthetic routes and methodologies, ultimately leading to the discovery of new compounds and applications.

InChI:InChI=1/C9H14O4/c10-9-7(4-6-12-9)13-8-3-1-2-5-11-8/h7-8H,1-6H2/t7-,8?/m0/s1

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 52079-23-9 (3S)-3-hydroxydihydrofuran-2(3H)-one 

Downstream Products

• 860795-17-1 (S)-1-{(S)-3-Benzyloxycarbonyl-3-[(S)-3-benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propylamino]-propyl}-azetidine-2-carboxylic acid 
• 77856-44-1 (S)-2-{[(S)-3-Benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-tert-butoxycarbonyl-amino}-4-oxo-butyric acid benzyl ester 
• 77856-43-0 (S)-2-{[(S)-3-Benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-tert-butoxycarbonyl-amino}-4-hydroxy-butyric acid benzyl ester 
• 77856-42-9 (S)-4-[tert-Butoxycarbonyl-((S)-2-oxo-tetrahydro-furan-3-yl)-amino]-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-41-8 (S)-4-((S)-2-Oxo-tetrahydro-furan-3-ylamino)-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-38-3 (S)-4-Oxo-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-47-4 (S)-1-((S)-3-Benzyloxycarbonyl-3-{[(S)-3-benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-tert-butoxycarbonyl-amino}-propyl)-azetidine-2-carboxylic acid benzyl ester 
• 77856-36-1 (S)-4-Hydroxy-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-44-1 2-{[3-Benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-tert-butoxycarbonyl-amino}-4-oxo-butyric acid benzyl ester 
• 77856-43-0 2-{[3-Benzyloxycarbonyl-3-(tetrahydro-pyran-2-yloxy)-propyl]-tert-butoxycarbonyl-amino}-4-hydroxy-butyric acid benzyl ester 
• 77856-42-9 4-[tert-Butoxycarbonyl-(2-oxo-tetrahydro-furan-3-yl)-amino]-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-41-8 4-(2-Oxo-tetrahydro-furan-3-ylamino)-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-38-3 4-Oxo-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 
• 77856-36-1 4-Hydroxy-2-(tetrahydro-pyran-2-yloxy)-butyric acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of the (9S, 18R)-seco acid of the leukocyte adhesion inhibitor cyclamenol A

Cyclamenol A is a naturally occurring inhibitor of leukocyte adhesion to endothelial cells. The (9S, 18R) diastereomer of cyclamenol A seco acid was synthesized by employing Sonogashira couplings and olefination reactions as the key steps. (C) 2000 Elsevier Science Ltd.

A short practical synthesis of 2′-deoxymugineic acid

A short and practical synthesis of 2′-deoxymugineic acid (DMA) has been developed via reductive alkylation with the aldehyde intermediates. No protection of azetidine-2-carboxylic acid was required and the presence of free carboxylic acid function facilitated purification by simple acid and base extractions. Furthermore, the intermediates were conveniently purified by HPLC due to the presence of chromophoric benzyl ester protecting group(s). Hydrogenolysis of the benzyl protecting groups in the final step furnished DMA in overall good yield.