Concomitant C-Ring Expansion and D-Ring Formation in Lanosterol Biosynthesis from Squalene without Violation of Markovnikov's Rule
Author:
Affiliation:
1. Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja026850r
Reference20 articles.
1. New insights into an old mechanism: [2 + 2] photocycloaddition of enones to alkenes
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3. Cyclization of a terpenoid diene with preformed A-B-D rings and its significance for the mechanism of terpenoid terminal epoxide cyclizations
4. Overall mechanism of terpenoid terminal epoxide polycyclizations
5. Generation of the onocerin system by lanosterol 2,3-oxidosqualene cyclase - implications for the cyclization process
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