16772-63-7

Usage

InChI:InChI=1/C15H22O4/c1-13(2)5-4-6-14(3)11(13)10(16)7-9-12(17)19-8-15(9,14)18/h7,10-11,16,18H,4-6,8H2,1-3H3/t10-,11+,14+,15-/m1/s1

Upstream product

• 23599-45-3 cinnamodial 
• 137266-37-6 (5aS,9aS,9bS)-6,6,9a-Trimethyl-3,5,5a,6,7,8,9,9a-octahydro-naphtho[1,2-c]furan-3,5,9b-triol 
• 121617-64-9 methyl (4S,4'S,4a'S,8a'S)-4'a,5',6',7',8',8'a-hexahydro-4'-hydroxy-5',5',8'a-trimethyl-2-oxospiro<1,3-dioxolane-4,1'(4'H)-naphthalene>-2'-carboxylate 
• 121701-36-8 C₁₆H₂₂O₄ 
• 121617-72-9 (1S,4aS,8aS)-2-[1,3]Dioxolan-2-yl-1-hydroxymethyl-5,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-ol 
• 121617-62-7 methyl (4S,4a'S,8a'S)-4'a,5',6',7',8',8'a-hexahydro-5',5',8'a-trimethyl-2-oxospiro<1,3-dioxolane-4,1'(4'H)-naphthalene>-2'-carboxylate 
• 121617-73-0 C₁₆H₂₂O₅ 
• 121617-61-6 (4S,4a'S,8a'S)-2'-(1,3-dioxolan-2-yl)-4'a,5',6',7',8',8'a-hexahydro-5',5',8a'-trimethylspiro<1,3-dioxolane-4,1'(4'H)-naphthalene>-2-one 
• 121617-63-8 methyl (4S,4a'S,8a'S)-4'a,5',6',7',8',8'a-hexahydro-5',5',8'a-trimethyl-2,2'-dioxospiro<1,3-dioxolane-4,1'(4'H)-naphthalene>-2'-carboxylate 
• 118244-95-4 (1S,4aS,8aS)-2-(1,3-dioxolan-2-yl)-1,4,4a,5,6,7,8,8a-octahydro-1-hydroxy-5,5,8a-trimethyl-1-naphthalenecarboxaldehyde 
• 137266-30-9 (3R,4S)-3-(2-Hydroxy-ethyl)-4-((1E,5E)-1,3,3-trimethyl-6-trimethylsilanyl-hexa-1,5-dienyl)-dihydro-furan-2-one 
• 137266-22-9 (4S,5S)-3,3-Dichloro-5-p-tolylsulfanyl-4-((1E,5E)-1,3,3-trimethyl-6-trimethylsilanyl-hexa-1,5-dienyl)-dihydro-furan-2-one 
• 74411-44-2 C₁₉H₂₅Cl₃O₇ 
• 74411-43-1 C₁₉H₂₃Cl₃O₇ 

Downstream Products

• 23599-46-4 (+/-)-cinnamosmolide 

Relevant academic research and scientific papers

STRUCTURE OF MUKAADIAL, A MOLLUSCICIDE FROM THE WARBURGIA PLANTS

The structure of a new sesquiterpene dialdehyde, mukaadial, isolated from Warburgia stuhlmannii and W. ugandensis and processing molluscicidal property, has been established by means of spectroscopic and chemical data.

Synthesis of (+)-fragolide and (-)-pereniporin B via vinylsilane terminated cationic cyclization

Enantioselective syntheses of (+)-fragolide and (-)-pereniporin B are detailed. Marino's lactone annulation method was employed to establish relative and absolute stereochemistry at carbon in the bicyclization substrate. Regio- and stereoselective oxidati

Synthesis of Mono- and Sesquiterpenoids, XVI - Synthesis of (-)-Pereniporins A and B, Sesquiterpene Antibiotics from a Basidiomycete

Starting from (S)-3-hydroxy-2,2-dimethyl-1-cyclohexanone (5), the enantioselective total syntheses of (-)-pereniporins A (1) and B (2) were achieved in 33 steps (0.6percent overall yield) and in 28 steps (1.8percent overall yield), respectively.

SYNTHESES OF (+/-)-CINNAMODIAL AND (+/-)-CINNAMOSMOLIDE

Syntheses of (+/-)-cinnamodial and (+/-)-cinnamosmolide were achieved starting from the intermediate used in the synthesis of (+/-)-warburganal.