(Q59484567)

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Stereoselective total synthesis of decarestrictine-J via Ring Closing Metathesis (RCM)

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Stereoselective total synthesis of decarestrictine-J via Ring Closing Metathesis (RCM) (English)

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1 reference

J.S. Yadav

1

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K. Anantha Lakshmi

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2

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N. Mallikarjuna Reddy

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3

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Attaluri R. Prasad

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4

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Basi V. Subba Reddy

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5

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publication date

2 January 2010

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published in

Tetrahedron

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volume

66

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page(s)

334-338

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1

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cites work

Secondary metabolites by chemical screening. 9. Decarestrictines, a new family of inhibitors of cholesterol biosynthesis from Penicillium. II. Structure elucidation of the decarestrictines A to D.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.45.66

Secondary metabolites by chemical screening. 8. Decarestrictines, a new family of inhibitors of cholesterol biosynthesis from Penicillium. I. Strain description, fermentation, isolation and properties.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.45.56

Secondary metabolites by chemical screening. 20. Decarestrictines, a new family of inhibitors of cholesterol biosynthesis from Penicillium: III. Decarestrictines E to M

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.45.1176

Secondary metabolites by chemical screening. Part 19. SM 196 A and B, novel biologically active angucyclinones from Streptomyces sp

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.44.670

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DOI

10.1016/J.TET.2009.10.100

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(Q59484567)

Stereoselective total synthesis of decarestrictine-J via Ring Closing Metathesis (RCM)

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