Desymmetrisation of meso-methylcyclooctanones. Highly enantioselective synthesis of C8 syn-isoprenoid and syn,syn-deoxypropionate subunits from a bicyclo[3.3.1]nonane precursor-Reference-Cited by-同舟云学术

Desymmetrisation of meso-methylcyclooctanones. Highly enantioselective synthesis of C8 syn-isoprenoid and syn,syn-deoxypropionate subunits from a bicyclo[3.3.1]nonane precursor

Published:2002-03 Issue:12 Volume:43 Page:2195-2198
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gambacorta Augusto,Tofani Daniela,Lupattelli Paolo,Tafi Andrea

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. A Microbial Lipase Based Stereoselective Synthesis of (d)-a-Tocopherol from (R)-Citronellal and (S)-(6-Hydroxy-2,5,7,8-tetramethylchroman-2-yl)acetic Acid

2. A Novel Route to Coenzyme Qn

3. Convenient highly stereoselective syntheses of (3R,7R,11R)- and (3S,7R,11R)-3,7,11,15-tetramethylhexadecanoic acid (phytanic acid) and the corresponding 3,7,11,15-tetramethylhexadecan-1-ols

4. Phytene-1,2-diol from Artemisia annua

5. Syntheses of 3,7-dimethylpentadecan-2-ols from intermediates formed from co-oligomerisation reactions of butadiene with diethyl malonate and acetaldehyde

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