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Literature DB >> 10891181

Revised constitution of sclerophytins A and B.

D Friedrich¹, R W Doskotch, L A Paquette.

Abstract

[structure: see text] Spectroscopic reevaluation of sclerophytin B, the acetate of sclerophytin A, has demonstrated unequivocally that these coral metabolites are not composed of two ether bridges.

Entities: Chemical

Mesh：

Substances：

Year: 2000 PMID： 10891181 DOI： 10.1021/ol000084g

Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005

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Cited

6 in total

1. A general route toward the synthesis of the cladiellin skeleton utilizing a SmI2-mediated cyclization.

Authors: Gary A Molander; Barbara Czakó; David J St Jean
Journal: J Org Chem Date: 2006-02-03 Impact factor: 4.354

2. Total syntheses of (+)-vigulariol and (-)-sclerophytin A.

Authors: Michael T Crimmins; Christina S Stauffer; Mark C Mans
Journal: Org Lett Date: 2011-08-19 Impact factor: 6.005

3. A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment.

Authors: Olivier Corminboeuf; Larry E Overman; Lewis D Pennington
Journal: J Org Chem Date: 2009-08-07 Impact factor: 4.354

Revised constitution of sclerophytins A and B.

1. A general route toward the synthesis of the cladiellin skeleton utilizing a SmI2-mediated cyclization.

2. Total syntheses of (+)-vigulariol and (-)-sclerophytin A.

3. A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment.

4. Synthesis and anticancer activity of sclerophytin-inspired hydroisobenzofurans.

5. Enantioselective synthesis of (-)-sclerophytin A by a stereoconvergent epoxide hydrolysis.

6. Cytotoxic and anti-inflammatory eunicellin-based diterpenoids from the soft coral Cladiella krempfi.