90695-44-6

Upstream product

• 86853-07-8 (2S,3R,4E)-(+)-3-Hydroxy-2-methyl-5-phenyl-4-pentensaeure-methylester 
• 479483-92-6 (E)-(2S,3R)-3-Hydroxy-2-methyl-5-phenyl-pent-4-enoic acid (S)-3-methyl-2-(toluene-4-sulfonylamino)-butyl ester 
• 90695-45-7 (2R,3R,4E)-(+)-3-Hydroxy-2-methyl-5-phenyl-4-pentensaeure-methylester 
• 70633-77-1 (3S,4E)-(+)-3-Hydroxy-5-phenyl-4-pentensaeure-methylester 
• 67498-12-8 (E)-(2S,3S)-3-Hydroxy-2-methyl-5-phenyl-pent-4-enoic acid methyl ester 
• 86853-06-7 Methyl 2-methyl-3-oxo-5-phenyl-4-pentenoate 
• 67498-12-8 (E)-syn-methyl 3-hydroxy-2-methyl-5-phenyl-4-pentanoate 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 82414-48-0 (E)-(2S,3R)-3-Methoxy-2-methyl-5-phenyl-pent-4-enoic acid 
• 88155-83-3 methyl (E)-(3R^*,4S^*)-4-methoxy-3-methyl-6-phenylhexa-5-enoate 
• 73341-71-6 (+/-)-oudemansin A 
• 73341-71-6 oudemansin A 
• 92979-23-2 C₂₆H₂₈O₂ 
• 90695-49-1 (+)-Oudemansin 
• 90664-03-2 (2R,3R,4E)-(-)-3-Methoxy-2-methyl-5-phenyl-4-penten-1-ol 
• 90664-07-6 (1E,3R,4S)-(+)-5-Brom-3-methoxy-4-methyl-1-phenyl-1-penten 
• 90664-05-4 (3R,4S,5E)-(+)-4-Methoxy-3-methyl-6-phenyl-5-hexennitril 
• 90695-47-9 (3R,4S,5E)-(-)-4-Methoxy-3-methyl-6-phenyl-5-hexensaeure-methylester 
• 90664-02-1 (1E,3R,4R)-(-)-3-Methoxy-4-methyl-5--1-phenyl-1-penten 
• 90695-50-4 (2E,3R,4S,5E)-methyl 4-methoxy-2-(methoxymethylene)-3-methyl-6-phenylhex-5-enoate 
• 90664-04-3 (2R,3R,4E)-(-)-(3-Methoxy-2-methyl-5-phenyl-4-pentenyl)-p-toluolsulfonat 
• 90664-01-0 (1E,3R,4R)-(+)-4-Methyl-5--1-phenyl-1-penten-3-ol 

Relevant academic research and scientific papers

Chelation-controlled ester-derived titanium enolate aldol reaction: Diastereoselective syn-aldols with mono- and bidentate aldehydes

A chelation-controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of (S)-valinol-derived ester with a variety of aldehydes proceeded with high syn-diastereoselectivities (up to 99:1) and isolated yields (94%).

Syntheses of (+)-Oudemansin and (+)-Epioudemansin Starting from Enantiomerically Pure Precursors; Absolute Configuration of the Naturally Occuring (-)-Oudemansin

The syntheses of the four optically pure methyl (E)-3-hydroxy-2-methyl-5-phenyl-4-pentenoates (+)- and (-)-5 as well as (+)- and (-)-6 were achieved by consecutive methylation and protonation of enolates, starting from (+)- and (-)-4.The esters (+)-6 and

STEREOSELECTIVE ADDITIONS TO CARBOXYLIC ACID DIANIONS AND β-LACTONE SUBSTITUTED ESTER ENOLATES. APPLICATION TO THE SYNTHESIS OF RACEMIC EPI-BLASTMYCINONE, δ-MULTISTRIATINE, PARACONIC ESTERS AND LIGNANTYPE DILACTONES

New stereoselective syntheses are reported for racemic 4-epi-blastmycinone (6) and δ-multistriatine (13) utilizing the anti-configurated γ,δ-unsaturated β-hydroxy-carboxylic acids 2a/b.A diastereo- and enantioselective aldoltype addition of phenylacetic acid dianion to benzaldehyde has been achaived by employing optically active alkoxide amide bases.Finally, highly stereocontrolled additions to the novel β-lactone substituted ester enolates 22 are described.