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Biosynthetic studies of marine lipids. 17. The course of chain elongation and desaturation in long-chain fatty acids of marine sponges

Journal of the American Chemical Society, 1988-11, Vol.110 (24), p.8117-8124

1988

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Fatty acids as biological markers for bacterial symbionts in sponges

Lipids, 1988-12, Vol.23 (12), p.1139-1145

1988

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Biosynthetic studies of marine lipids. 9. Stereochemical aspects and hydrogen migrations in the biosynthesis of the triply alkylated side chain of the sponge sterol strongylosterol

Journal of the American Chemical Society, 1986-12, Vol.108 (26), p.8235-8241

1986

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Biosynthetic studies of marine lipids. 20. Sequence of double-bond introduction in the sponge sterol 24.beta.-methylcholesta-5,7,22,25-tetraen-3.beta.-ol

Journal of organic chemistry, 1989-03, Vol.54 (7), p.1642-1647

1989

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Biosynthetic studies of marine lipids. 14. 24(28)-Dehydroaplysterol and other sponge sterols from Jaspis stellifera

Journal of organic chemistry, 1988-07, Vol.53 (15), p.3466-3469

1988

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Biosynthetic studies of marine lipids 18. Biosynthesis of 3β-(hydroxymethyl)-A-nor-5α-cholest-15-ene in the marine sponge phakellia aruensis

Tetrahedron letters, 1988, Vol.29 (33), p.4081-4084

1988

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Biosynthetic studes of marine lipids 7 : Experimental demonstration of a double alkylation at c-28 in the biosynthesis of 24-isopropylcholesterols in a sponge

Tetrahedron, 1986, Vol.42 (15), p.4147-4155

1986

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Biosynthetic studies of marine lipids 16. De novo sterol biosynthesis in sponges. Incorporation and transformation of cycloartenol and lanosterol into unconventional sterols of marine and freshwater sponges

Tetrahedron, 1989, Vol.45 (7), p.1893-1904

1989

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Cell membrane localization of sterols with conventional and unusual side chains in two marine demonsponges

Lipids, 1988-08, Vol.23 (8), p.750-754

1988

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Biosynthetic studies of marine lipids 10. Double side chain extension in the triply alkylated sponge sterol xestosterol

Tetrahedron letters, 1986, Vol.27 (40), p.4821-4824

1986

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Isoprenoid biosynthesis in a marine sponge of the Amphimedon genus: incorporation studies with [1-14C] acetate, [4-14C] cholesterol and [2-14C] mevalonate

Comparative biochemistry and physiology. B, Comparative biochemistry, 1988, Vol.91 (2), p.293-300

1988

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Biosynthetic studes of marine lipids 7

Tetrahedron, 1986-01, Vol.42 (15), p.4147-4155

1986

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Biosynthetic studies of marine lipids 12

Tetrahedron, 1987, Vol.43 (10), p.2213-2222

1987

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Biosynthetic studies of marine lipids 12. : Biosynthesis in marine sponges of sterois possessing the δ5,7-nucleus typical of fungi and the 24-alkyl side chain characteristic of plants

Tetrahedron, 1987, Vol.43 (10), p.2213-2222

1987

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Synthesis of a triaromatic steroid biomarker. (20R,24R)-4,17β-dimethyl-18,19-dinorstigmasta-1,3,5,7,9,11,13-heptaene, from stigmasterol

Journal of organic chemistry, 1994-02, Vol.59 (4), p.926-928

1994

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Synthesis of Biomarkers in Fossil Fuels. 8. Synthesis of a Triaromatic Steroid Biomarker, (20R,24R)-4,17.beta.-Dimethyl-18,19-dinorstigmasta-1,3,5,7,9,11,13-heptaene, from Stigmasterol

Journal of organic chemistry, 1994-02, Vol.59 (4), p.926-928

1994

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1H and 13C NMR analysis of C-23 and C-24 diastereomers of 5α-dinosterane

Magnetic resonance in chemistry, 1994-02, Vol.32 (2), p.101-106

1994

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1 H and 13 C NMR analysis of C‐23 and C‐24 diastereomers of 5α‐dinosterane

Magnetic resonance in chemistry, 1994-02, Vol.32 (2), p.101-106

1994

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Vitaliĭ Sergeevich Zuev (on his fiftieth birthday)

Soviet journal of quantum electronics, 1983-07, Vol.13 (7), p.998-999

1983

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Biosynthetic studies of marine lipids. 17. The course of chain elongation and desaturation in long-chain fatty acids of marine sponges

Fatty acids as biological markers for bacterial symbionts in sponges

Biosynthetic studies of marine lipids. 9. Stereochemical aspects and hydrogen migrations in the biosynthesis of the triply alkylated side chain of the sponge sterol strongylosterol

Biosynthetic studies of marine lipids. 20. Sequence of double-bond introduction in the sponge sterol 24.beta.-methylcholesta-5,7,22,25-tetraen-3.beta.-ol

Biosynthetic studies of marine lipids. 14. 24(28)-Dehydroaplysterol and other sponge sterols from Jaspis stellifera

Biosynthetic studies of marine lipids 18. Biosynthesis of 3β-(hydroxymethyl)-A-nor-5α-cholest-15-ene in the marine sponge phakellia aruensis

Biosynthetic studes of marine lipids 7 : Experimental demonstration of a double alkylation at c-28 in the biosynthesis of 24-isopropylcholesterols in a sponge

Biosynthetic studies of marine lipids 16. De novo sterol biosynthesis in sponges. Incorporation and transformation of cycloartenol and lanosterol into unconventional sterols of marine and freshwater sponges

Cell membrane localization of sterols with conventional and unusual side chains in two marine demonsponges

Biosynthetic studies of marine lipids 10. Double side chain extension in the triply alkylated sponge sterol xestosterol

Isoprenoid biosynthesis in a marine sponge of the Amphimedon genus: incorporation studies with [1-14C] acetate, [4-14C] cholesterol and [2-14C] mevalonate

Biosynthetic studes of marine lipids 7

Biosynthetic studies of marine lipids 12

Biosynthetic studies of marine lipids 12. : Biosynthesis in marine sponges of sterois possessing the δ5,7-nucleus typical of fungi and the 24-alkyl side chain characteristic of plants

Synthesis of a triaromatic steroid biomarker. (20R,24R)-4,17β-dimethyl-18,19-dinorstigmasta-1,3,5,7,9,11,13-heptaene, from stigmasterol

Synthesis of Biomarkers in Fossil Fuels. 8. Synthesis of a Triaromatic Steroid Biomarker, (20R,24R)-4,17.beta.-Dimethyl-18,19-dinorstigmasta-1,3,5,7,9,11,13-heptaene, from Stigmasterol

1H and 13C NMR analysis of C-23 and C-24 diastereomers of 5α-dinosterane

1 H and 13 C NMR analysis of C‐23 and C‐24 diastereomers of 5α‐dinosterane

Vitaliĭ Sergeevich Zuev (on his fiftieth birthday)

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