13266-02-9

Usage

Chemical Properties

White Solid

Uses

Wittig Reagents.

Upstream product

• 13362-52-2 1,13-tridecanediol 
• 116754-58-6 13-bromo-1-tridecylalcohol 
• 603-35-0 triphenylphosphine 
• 28267-29-0 ethyl tridecanoate 
• 671787-02-3 (E)-Tridec-2-enoic acid ethyl ester 
• 112-44-7 undecylaldehyde 
• 544-63-8 n-tetradecanoic acid 

Downstream Products

• 105265-47-2 3-O-benzyl-(Z)-5,6-dehydro-5,6,7,8,9,10,11,12,13,14,15,16,17,18-tetradecadeoxy-1,2-O-isopropylidene-α-D-xylo-octadecofuranose 
• 471891-18-6 (2S,3S,4R,5Z)-2-azido-3,4-dibenzyloxy-5-octadecen-1-ol 
• 129779-77-7 (2S,3S,4R)-1,3,4-tri-O-benzyl-2-amino-1,3,4-octadecanetriol 
• 129779-76-6 (2S,3S,4R)-1,3,4-tri-O-benzyl-2-azido-1,3,4-octadecanetriol 
• 129831-88-5 (2R,3S,4R)-1,3,4-tri-O-benzyl-2-O-methansulfonyl-1,2,3,4-octadecanetetraol 
• 129779-78-8 (2S,3S,4R)-1,3,4-tri-O-benzyl-N-tetracosanoyl-2-amino-1,3,4-octadecanetriol 
• 164988-68-5 (2R,3S,4R)-1,3,4-Tris-benzyloxy-octadecan-2-ol 
• 209899-68-3 (2S,3S,4R)-2-(N-hexacosanoylamino)-3,4-di-O-benzoyl-1,3,4-octadecanetriol 
• 1053701-00-0 (2S,3S,4R)-2-(N-hexacosanoylamino)-1-O-(triphenylmethyl)-1,3,4-octadecanetriol 
• 148289-66-1 C₅₈H₉₅NO₈ 
• 164988-99-2 Acetic acid (R)-1-((1S,2S,3R)-2,3-dihydroxy-1-trityloxymethyl-heptadecylcarbamoyl)-tricosyl ester 
• 1054644-79-9 Hexacosanoic acid ((1S,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-heptadecyl)-amide 
• 164989-00-8 Acetic acid (R)-1-((1S,2S,3R)-2,3-dihydroxy-1-trityloxymethyl-heptadecylcarbamoyl)-pentacosyl ester 
• 164988-85-6 Acetic acid (R)-1-((1S,2S,3R)-2,3-bis-benzyloxy-1-benzyloxymethyl-heptadecylcarbamoyl)-tricosyl ester 

Relevant academic research and scientific papers

Method for synthesizing Micromelalopha troglodyta sex pheromone active ingredient

The invention relates to the technical field of insect sex pheromone component synthesis, and provides a novel method for synthesizing Micromelalopha troglodyta sex pheromone active ingredient. According to the novel method, 1, 13-tridecanol is used as an

NOVEL GLYCINE TRANSPORT INHIBITORS FOR THE TREATMENT OF PAIN

The present invention relates to novel glycine transport inhibitor compounds and their use for treating pain.

Total synthesis of N,O,O,O-tetraacetyl-d-ribo-phytosphingosine and its 2-epi-congener

Total synthesis of the natural d-ribo-phytosphingosine I and its 2-epimer III in the protected form was achieved through a common strategy. The aza-Claisen rearrangement of allylic thiocyanate (Z)-V incorporated the new stereogenic centre with nitrogen and the subsequent Wittig olefination constructed a non-polar side chain. Hydrogenation, followed by removal of protecting groups, completed the syntheses of I and III.

An efficient and stereoselective synthesis of (2R,2′S)-1-O-(2′-hydroxyhexadecyl)glycerol and its oxo analogs: Potential antitumour compounds from Shark Liver Oil

Reproducible, high-yielding, cost efficient, regio- and stereoselective synthesis of the title compound 3 isolated from Shark Liver Oil has been described. The compound 3 is prepared in an overall yield of 41% from chiral synthon 4 by the sequential reaction of 4 with C-13 Wittig salt; hydrogenation; epoxidation and regioselective opening. The oxo analogs 18 and 19 are prepared from four different achiral synthons by the sequential regioselective opening of the corresponding epoxide with different alcohols, methylation and deprotection strategies. Copyright