Isolation ofΔ9(11)-sterols from the sea cucumber psolusfabricii. Implications for holothurin biosynthesis

- 14α-Methyl-5α-cholest-9(11)-en-3β-ol ($\text{2}$) and 4α,14α-dimethyl-5α-cholest-9(11)-en-3β-ol ($\text{3}$) have been isolated from the sea cucumber $\text{Psolus}$$\text{fabricii}$ and characterised by ¹H NMR, ¹³C NMR and mass spectrometry. Lanost-9(11)-en-3β-ol ($\text{4}$) has also been tentatively identified. The relevance of this series of Δ⁹⁽¹¹⁾-sterols to holothurin biosynthesis is briefly discussed.     

Isolation and synthesis of 1-methylisoguanosine,a potent pharmacologically active constituent from the marine sponge tenadiadigitata

A new pharmacologically active agent isolated from the marine sponge $\text{Tedania}$$\text{digitata}$ has been identified as 1-methylisoguanosine ($\text{1}$) by spectral and degradative chemical methods and synthesis from a β-D-ribofuranosylimidazole ($\text{2}$).     

Stereoselective synthesis of (1R,3R,5S-1,3-dimethyl-2,9-dioxabicyclo[3.3.1]nonane

(1$\text{R}$,3$\text{R}$,5$\text{S}$)-1,3-Dimethyl]-2,9-dioxabicyclo[3.3.1]nonane $\text{1}$ has been stereoselectively synthesized based on a highly stereoselective method for the synthesis of 1,3-$\text{syn}$-polyol.     

(10R̃, 11R̃)-(+)-squalene-10, 11-epoxide: Isolation from Laurencia okamurai and the asymmetric synthesis

From a red alga $\text{Laurencia okamurai}$ (10$\text{R}\text{?}$, 11$\text{R}\text{?}$)-(+)-squalene-10, 11-epoxide $\text{1}\text{?}$ was isolated and its asymmetric synthesis has been achieved starting from $\text{trans, trans}$-farnesol.     

Yield of I(2Psol:12) in the photodissociation of CH2I2

The production of I(²P_{$\text{1}\text{2}$}) in the photolysis of CH₂I₂ has been studied optoacoustically at excitation wavelengths between 365.5 and 247.5 nm. Bands found at 32200 and 47000 cm^?1 correlate with I(²P_{$\text{3}\text{2}$}) whilst those at 34700 and 40100 cm^?1, which correlate with I(²P_{$\text{1}\text{2}$}), give final ²P_{$\text{3}\text{2}$}/²P_{$\text{1}\text{2}$} ratios of 1.75 and 1.1, respectively, after curve crossing.     

1,6-dihydro-3(2H)-pyridinones as synthetic intermediates. Total synthesis of (±)-tecomanine

The first and stereoselective total synthesis of (±)-tecomanine ($\text{1}$) has been achieved from ethyl 1,6-dihydro-3(2H)-pyridinone-1-carboxylate ($\text{2}$) as a synthon.     

Comparison of reactivity of Ar(3Po) and Ar(3P2) metastable states. Products of quenching by some halogen-containing compounds

Vacuum UV emission from the products of quenching ofAr(³P_o) and Ar(³P₂) by several reagents has been compared. The large differences suggest that Ar(³P_o) and Ar(³P₂) preferentially yield respectively the D($\text{1}\text{2}$) and B($\text{1}\text{2}$) excited states of ArBr^★ or ArCl^★, which show specific, but very different, predissociation patterns.     

Total synthesis of (+--oudemansin

($\text{+}\text{-}$)-Oudemansin has been synthesized starting from $\text{trans}$-cinnamaldehyde by a route involving the stereoselective Zn(BH₄)₂ reduction of β-keto ester.     

Total synthesis of slow reacting substances (SRS's): 6-epi-leukotriene C and 6-epi-leukotriene D

6-$\text{Epi}$-leukotrienes C and D (3 and 4) have been synthesized unambiguously via the 5($\text{S}$), 6($\text{R}$)-epoxide (5,6-$\text{cis}$) which is isomeric with leukotriene A. These 6-$\text{epi}$-leukotrienes are less active (especially 4) than leukotrienes C and D (1 and 2) and have not been found in substantial quantity in natural SRS sources.     

Steroidal antifeedants from the dorid nudibranch Aldisasanguineacooperi

Two steroids, 3-oxo-chol-4-ene-24-oic acid ($\text{2}$) andi ts unsaturated analog $\text{4}$ have been isolated from the dorid nudibranch $\text{Aldisa}$$\text{sanguinea}$$\text{cooperi}$, and the acid $\text{2}$ has been shown to have antifeedant properties.     

Isolation of aspirochlorine (=antibiotic A30641) possessing a novel dithiodiketopiperazine structure from Aspergillus Flavus

A very unusual dithiokikeptopiperazine structure ($\text{1}$) has been assigned to aspiroclorine, C₉H₁₂N₂O₅S₂Cl, produced as a biologically active substance together with canadensolide by $\text{Aspergillus}$$\text{flavus}$, which has been found to be identical with the antibiotic A 30641 from $\text{A.}$$\text{tamarii}$.     

The structure of tatsinine,a novel c19-diterpenoid alkaloid from delphinium tatsienense franch

A novel C₁₉-diterpenoid alkaloid designated as tatsinine has been isolated from the roots of $\text{Delphinium}$$\text{tataienence}$ and its structure (3) has been derived from ¹H NMR and ¹³C NMR spectroscopic evidence.     

Synthesis of N-benzoyl L- and D-2,3,6-trideoxy-3-aminoxylo-hexose from non-carbohydrate precursors

The enantiomeric alcohols ($\text{2}$) and ($\text{11}$), obtained from (2$\text{R}$,3$\text{R}$) tartaric acid and, respectively, $\text{L}$-threonine, have been used to construct the C₆, enantiomeric deoxy amino sugar derivatives ($\text{7}$) and ($\text{12}$)     

Isolation of sterols with cyclopropyl-containing side chains from the cultured marine alga peridiniumfoliaceum

The sterol fraction of the cultured dinoflagellate $\text{Peridinium}$$\text{foliaceum}$ contains in addition to cholesterol, 24-methylcholesterol, 4,24-dimethylcholesterol and dinosterol ($\text{3c}$) small amounts of the cyclopropyl-containing sterols gorgosterol ($\text{1a}$) and 5α-gorgostanol ($\text{1b}$) as well as 4α-methylgorgostanol ($\text{1c}$) and E-4α,22ξ,23ξ (or 24ξ)-trimethylcholest-17(20)-en-3β-ol ($\text{6c}$ or $\text{7c}$). The biosynthetic implications of the first isolation of such sterols from a free-living alga are emphasized.     

Conformational behaviour and inclusion compound forming properties of 5,18-disubstituted derivatives of 5, 11, 12, 18-tetrahydrotribenzo[b,f,j][1,4]diazacyclododecine-6, 17-dione

An X-ray structure analysis shows that the 5, 18-dimethyl derivative ($\text{5}$) of the title compound ($\text{4}$) crystallises from xylene as a 1:1 inclusion compound in which the host molecules adopt propeller-like conformations ($\text{7}$ and $\text{7}$*) with almost perfect $\text{C}$₂ symmetry. Dynamic ¹H n.m.r. spectroscopy shows that the 5, 18-dibenzyl derivative ($\text{6}$) of ($\text{4}$) forms a 1:1 inclusion compound with ethanol in the solid state and undergoes ring inversion ($\text{7}$ ? $\text{7}$*) between enantiomeric propeller-like conformations in solution against a barrier of 21.1 kcal mol^?1     

Electronic spectra of 12-S-CIS conformationally locked retinals

The electronic absorption spectra of the four new 12-$\text{s}$-$\text{cis}$-locked retinals (1a–1d) bearing 7-$\text{trans}$, 11-$\text{trans}$ double bond geometries are described and compared with those of analogous 7-$\text{trans}$, 11-$\text{cis}$-geometries (1e–1h) and parent retinals (2a-h).     

Biogenetic-type synthesis of (±)-dictyopterene A,an odoriferous substance obtained from brown seaweeds, Dictyopteris

Biogenetic-type synthesis of (±)-dictyopterene A ($\text{1}$) was achieved employing 1,$\text{cis}$-5-undecadien-3-ol ($\text{2}$) postulated to be a biosynthetic intermediate of $\text{1}$: this synthesis means that transformation of dictyoprolene ($\text{4}$) into dictyopterene A ($\text{1}$) was formally made.     

Derivatives and reactions of glutacondialdehyde IV 1-substituted-3-formyl-2(1H)-pyridinethiones

The reaction of the glutacondialdehyde anion with alkyl and acyl isothiocyanates has been investigated. Whereas alkyl isothiocyanates give rise to 1-alkyl-3-formyl-2(1$\text{H}$)-pyridinethiones, $\text{O}$-acylated glutacondialdehyde derivatives are formed from acyl isothiocyanates in most cases. The reaction courses may be understood on the basis of the principle of hard and soft acids and bases.     

Synthesis and 13C nmr characterization of some π-excessive heteropolyaromatic compounds

Several π-excessive heteropolyaromatic compounds, which contain furan and thiophen ring and are possible antifungal agents, have been synthesized in good yields according to two general methods. The first method has been used to prepare compounds possessing thiophens linked by their 2- and 5-positions, such as the ter-aryls $\text{2b}$, $\text{2d}$ and $\text{2a}$. Two precursors of these compounds have been obtained either by the Glaser reaction, or using a novel Pd-mediated reaction. The second method,which consists of the Ni-or Pd-catalyzed heteroarylation of heteroarene halides via cross-coupling with heteroaryl Grignard reagents or zinc halides,has been used to prepare the bi-aryls $\text{1a-e}$, which contain two heteroaromatic units, and the ter-aryl $\text{2c}$. Compound $\text{1e}$ has been also prepared starting from 2-(2-thienyl) furan ($\text{1c}$) by selective lithiation, followed by bromination.The ¹³C NMR signals of $\text{1a-e}$ and $\text{2a-d}$ have been assigned on the basis of the literature data and by relaxation measurements. Relaxation data have been also used to obtain qualitative informations on the conformational equilibria of the bi-aryls $\text{1a}$, $\text{1c}$ and the ter-aryls $\text{2a-d}$.     

Stereochemistry of electrophilic addition to dimethyl tricyclo[4,2,2,02,5] Deca-3,7-diene-9,10-dicarboxylate. Molecular structure of Hg(OAc)2-addition product

The molecular structure of the $\text{trans}$ addition product of Hg(OAc)₂ to diester $\text{1}$ has been determined by X-ray diffraction (represented by formula $\text{3}$) which leads to a revision of previously claimed $\text{cis}$-additions in this series.