57794-67-9

Upstream product

• 18444-84-3 (5S^*,10R^*)-6,10-dimethylspiro<4.5>dec-6-en-2-one 
• 79265-79-5 (8S,10S,13R)-7,13-Dimethyl-1,4-dithia-dispiro[4.2.4.2]tetradec-6-en-10-ol 
• 928203-23-0 2-(3-hydroxy-hex-4-enoyl)-cyclopentanone 
• 58150-20-2 6-methyl-10-oxo-spiro[4.5]decane-2-carboxylic acid methyl ester 
• 928203-32-1 6-hydroxy-10-methyl-spiro[4.5]dec-1-ene-2-carboxylic acid methyl ester 
• 120-92-3 cyclopentanone 
• 155528-07-7 (+)-(3R,4E)-3-(tert-butyldimethylsilyloxy)hex-4-enal 
• 928203-24-1 2-propenyl-2,3,6,7-tetrahydro-5H-cyclopenta[b]pyran-4-one 
• 57766-74-2 6-methyl-10-methylene-spiro[4.5]decane-2-carboxylic acid methyl ester 
• 51388-76-2 (2S^*,5S^*,10R^*)-6,10-dimethylspiro<4.5>dec-6-en-2-ol 
• 81346-18-1 (5S^*,10R^*)-3-chloro-6,10-dimethylspiro<4.5>deca-2,6-diene-2-carbaldehyde 
• 186581-53-3 diazomethane 
• 81346-20-5 (2RS,5R^*,10R^*)-6,10-dimethylspiro<4.5>dec-6-ene-2-carboxylic acid 
• 928203-31-0 6-(tert-butyl-dimethyl-silanyloxy)-10-methyl-spiro[4.5]dec-1-ene-2-carboxylic acid methyl ester 

Downstream Products

• 59331-07-6 (+/-)-hinesol 
• 1460-73-7 2-[(3R,5R,6R)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-ol 
• 1460-73-7 (±)-agarospirol 
• 1460-73-7 (2RS,5SR,10SR)-hinesol 

Relevant academic research and scientific papers

Claisen rearrangement strategy in alkenyl dihydropyran leading to total synthesis of (+)-α-vetispirene and (-)-agarospirol

Total synthesis of (+)-α-vetispirene and (-)-agarospirol based on a Claisen rearrangement has been achieved. This is the first example of a Claisen rearrangement in an enantio-enriched alkenyl bicyclic dihydropyran system with perfect asymmetric transmission. Copyright

Connective synthesis of spirovetivanes: Total synthesis of (±)-agarospirol, (±)-hinesol and (±)-α-vetispirene

A concise, connective synthesis of naturally occurring spirovetivanes 1 and 3, in racemic form, is presented. This novel approach involves the efficient assembly of the advanced intermediate 12 through a unique spiroannulation protocol. Wiley-VCH Verlag GmbH & Co. KGaA1 69451 Weinheim, Germany, 2004.

A New Synthesis of (+/-)-Agarospirol and (+/-)-Hinesol

(+/-)-Agarospirol (8) and (+/-)-hinesol (9) were simultaneously synthesized via a useful synthon in the synthesis of spirovetivane-type sesquiterpenes, i.e., (2S*,5S*,10R*)-2-hydroxy-6,10-dimethylspirodec-6-en-8-one (1), which had previously been prepared from the corresponding phenolic α-diazoketone via the spiro-annelation reaction and subsequent stereo-controlled Birch reduction, both reported in our previous communications.Keywords-(+/-)-agarospirol; (+/-)-hinesol; spirovetivane-type sesquiterpenes; useful synthon; (2S*,5S*,10R*)-2-hydroxy-6,10-dimethylspirodec-6-en-8-one