NMR study on 9‐S and 9‐R oxirane derivatives of ascomycin

Structure elucidation of 9‐S and 9‐R oxirane derivatives of ascomycin, a 23‐membered immunomodulating macrolactam, was performed using NMR spectroscopy. The total ¹H and ¹³C signal assignments required the gradient‐selected versions of COSY (gs‐COSY), heteronuclear multiple quantum‐correlation spectroscopy (gs‐HSQC), heteronuclear multiple‐bond correlation spectroscopy (gs‐HMBC), and nuclear Overhauser methods. The data sets then were used to examine the dependence of ketone–hemiketal and cis–trans amide equilibria on the substitution pattern and the absolute configuration of the chiral oxirane. Copyright © 2002 John Wiley & Sons, Ltd.     

立体选择性合成2-(a-噻吩甲酰基)-3-取代苯基-4-乙氧羰基-5-甲基-反式-2,3-二氢呋喃

溴化(a-噻吩甲酰基)甲基三苯鉮1与3-取代苯甲叉基-2,4-戊二酮 2以碳酸钾为碱,在苯中55℃条件下反应,可以较好的收率、高立体选择性地生成反-2-(a-噻吩甲酰基)-3-取代苯基-4-乙氧羰基-5-甲基-2,3-二氢呋喃3。产物结构均经波谱予以确定。本文还提出了生成产物的可能机理。     

A New Alkaloid from the Seeds of Sophora alopecuroides L.

Alopecurin A, an alkaloid with an unprecedented skeleton, was isolated from the seeds of Sophora alopecuroides L. The absolute configuration and structure of this compound was identified as (3S,12R)‐3‐hydroxy‐1,7‐diazatricyclo[10.4.0.1^3,7]heptadecane‐11,16,17‐trione (=(7S,15aR)‐decahydro‐7‐hydroxy‐6H‐7,11‐methano‐4H‐pyrido[1,2‐a][1,7]diazacyclododecine‐4,15,16(12H)‐trione). The structure and absolute configuration was elucidated by spectroscopic methods, mainly HR‐ESI‐TOF‐MS, IR, 1D‐NMR (¹H‐ and ¹³C‐NMR), 2D‐NMR (COSY, NOESY, HSQC, HMBC), and particularly X‐ray crystal‐diffraction and CD spectral analysis.     

Structure elucidation of [1,3]oxazolo[4,5‐e][2,1]benzisoxazole and naphtho[1,2‐d][1,3]‐ and phenanthro[9,10‐d]oxazoles using gradient selected gHMBC,gHMQC and gHMQC‐TOCSY NMR techniques

Structure elucidation of compounds in the benzisoxazole series ( 1 – 6 ) and naphtho[1,2‐d][1,3]‐ ( 7 – 10 ) and phenanthro[9,10‐d][1,3]oxazole ( 11 – 14 ) series was accomplished using extensive 2D NMR spectroscopic studies including ¹H–¹H COSY, long‐ range ¹H–¹H COSY, ¹H–¹³C COSY, gHMQC, gHMBC and gHMQC‐TOCSY experiments. The distinction between oxazole and isoxazole rings was made on the basis of the magnitude of heteronuclear one‐bond ¹J_{C2, H2} (or ¹J_{C3, H3}) coupling constants. Complete analysis of the ¹H NMR spectra of 11 – 14 was achieved by iterative calculations. Gradient selected gHMQC‐TOCSY spectra of phenanthro[9,10‐d][1,3]oxazoles 11 – 14 were obtained at different mixing times (12, 24, 36, 48 and 80 ms) to identify the spin system where the protons of phenanthrene ring at H‐5, H‐6 and at H‐9 and H‐7 and H‐8 were highly overlapping. Copyright © 2003 John Wiley & Sons, Ltd.     

首次合成来源于鼠李属植物中的两个新颖的蒽环鼠李糖苷，2’, 3’-Di-O-acetylfrangulin A 和 Prinoidin

首次全合成来源于鼠李属植物中的两个天然产物2’, 3’-di-O-acetylfrangulin A (1) 和 prinoidin (2),它们对KB细胞表现出较好的细胞毒活性。通过1H NMR, 13C NMR, 1H-1H COSY, HMQC 和 HMBC确证了两个化合物的结构。     

Marrusidins A and B,New Epimeric Labdane Diterpenes from Marrubium anisodon

Marrusidins A ( 1 ) and B ( 2 ), two new labdane‐type diterpenes, were isolated from the CHCl₃‐soluble subfraction of Marrubium anisodon, along with polyodonine. Their structures were assigned with the aid of ¹H‐ and ¹³C‐NMR spectra and by COSY, HMQC, NOESY, and HMBC experiments.     

Lyciumaside and Lyciumate: A New Diacylglycoside and Sesquiterpene Lactone from Lycium shawii

One new diacylglycoside named lyciumaside ( 1 ) and a new sesquiterpene lactone named lyciumate ( 2 ) were isolated from Lycium shawii Roem . & Schult . The structures of the two new compounds were elucidated based on 1D‐ (¹H‐ and ¹³C‐NMR and NOE) and 2D‐NMR (COSY, HSQC, and HMBC) spectroscopic techniques, and mass spectrometry (ESI‐MS). Preliminary evaluations demonstrated lyciumaside ( 1 ) possesses strong antioxidant activity with an IC₅₀ = 30 μg/ml (80% inhibition) while it was inactive in α‐glucosidase and urease enzymes assays.     

Chemoselectivity and Conformational Analysis of the Reaction of 2‐Acetylcycloalkanones with Benzohydrazide: Synthesis and Reduction of 1‐Aroylcycloalkapyrazole Derivatives

From the reaction of 2‐acetylcyclopentanone and 2‐acetyl‐2‐methylcyclopentanone with benzohydrazide, the 1‐benzoyl‐6a‐hydroxycyclopentapyrazole derivatives 2a and 2b were obtained as the only reaction products, whereas from the reaction of 2‐acetylcyclohexanone an epimeric cis/trans mixture of the 2‐benzoyl‐3‐hydroxy‐2H‐indazole derivative 3c was formed. The dehydration of the isolated compounds 2a and 3c , as well as the NaBH₄ and NaBH₃CN reduction products of 2a were studied. The structural assignments of the compounds derived were established by analysis of their NMR spectra (¹H, ¹³C, DEPT, COSY, NOESY, HETCOR C? H, and COLOC C? H). The chemoselectivity of the reactions of 1a and 1c with benzohydrazide was studied by conformational analysis with MM2 and semiempirical (AM1 and PM3) MO calculations.     

Phlomisamide and Phlomisteriod: A New Ceramide and a New Stigmasterol Derivative from Phlomis cashmeriana

Phlomisamide ( 1 ), a new ceramide, and a new stigmasterol derivative, phlomisteriod ( 2 ), have been isolated from Phlomis cashmeriana. Their structures were elucidated by comprehensive analysis of their 1D‐ (¹H‐ and ¹³C‐NMR) and 2D‐NMR (COSY, HMQC, HMBC), and HR‐EI‐MS data.     

A new stereoisomer of stemmadenine alkaloid from Tabernaemontana heyneana

A new alkaloid, 15‐β‐stemmadenine, was isolated from the fruits of Tabernaemontana heyneana Wall. from the ethanolic extract. The complete ¹H and ¹³C NMR assignments of the compound were carried out using COSY, HMQC and HMBC. Stereochemistry at C‐15 and C‐16 was established using ROESY and temperature‐dependent ¹H NMR studies. Copyright © 2002 John Wiley & Sons, Ltd.     

A New Dimeric Secoiridoid Glycoside from the Leaves of Olea ferruginea Royle

A new dimeric secoiridoid glycoside, trivially named oleferrugine B ( 1 ), has been isolated from the AcOEt‐soluble part of the MeOH extract of leaves of Olea ferruginea Royle . The structure of the isolated compound was established on the basis of ESI‐MS fragmentation patterns, and 1D‐ and 2D‐NMR techniques, including ¹H‐ and ¹³C‐NMR, HSQC, ¹H,¹H‐COSY, HMBC, and NOESY experiments, and by comparison with literature data.     

1,3‐Dipolar Cycloaddition Reactions Leading to the Synthesis of New 2,3,5‐Triaryl‐4H,2,3,3a,5,6,6a‐hexahydropyrrolo[3,4‐d]isoxazole‐4,6‐diones

Cycloaddition of C,N‐diphenylnitrones 1 to N‐aryl maleimides 2 afforded two diastereomeric isoxazolidines with high selectivity. The structure and steric configuration of the adducts have been assigned on the basis of ¹H NMR, ¹H NMR COSY, ¹³C NMR and IR spectroscopy. The π–π stacking interactions between maleimide's and nitrone's aromatic rings during the 1,3‐dipolar cycloaddition were assumed to control the exo–endo selectivity of the reaction. Thus, the exo–endo ratio depends upon the position of the substituent present on the C‐phenyl ring of the C,N‐diphenylnitrones.     

Coagulansins A and B,New Withanolides from Withania coagulans Dunal

Coagulansins A ( 1 ) and B ( 2 ), two new withanolides, were isolated from the CHCl₃‐soluble fraction of Withania coagulans Dunal , along with two known withanolides, coagulin R and withanolide P. Their structures were assigned by means of ¹H‐ and ¹³C‐NMR spectra, DEPT, and ¹H,¹H‐COSY, NOESY, HMQC, and HMBC experiments.     

Unexpected Spiroproducts from the Reaction of N‐Benzoylglycine with Ortho‐Formylbenzoic Acids −3,5′‐Dioxo‐2′‐Phenyl‐1,3‐Dihydrospiro[Indene‐2,4′‐[1,3]Oxazol]‐1‐yl Acetates: Establishments of Their Structure

This paper describes a method of preparation of new 3,5′‐dioxo‐2′‐phenyl‐1,3‐dihydrospiro[indene‐2,4′‐[1,3]oxazol]‐1‐yl acetate and its 5‐chloro‐ and bromoderivatives as products of interaction of N‐benzoylglycine (hippuric acid) with corresponding ortho‐formylbenzoic acids. The reaction carried out in acetic anhydride media in the presence of piperidine as catalyst. The novel spirocompounds were purified by column chromatography from multicomponent reaction mixtures. The composition of the spiro‐products was confirmed by C, H, N element analysis. The structure was established by IR, MS, ¹H‐ and ¹³C‐NMR analysis including COSY ¹H‐¹³C experiments.     

A simple and efficient preparation of pyrazolo[3,4‐b]‐pyridine derivatives through an unexpected reaction of cyanothioacetamide under microwave irradiation

An unexpected multicomponent reaction of cyanothioacetamide with aromatic aldehydes and aminopyrazole under MWI was found and reported. It turned out to be an efficient and simple procedure for the preparation of pyrazolo[3,4‐b]pyridine derivatives. The structure of the product was characterized by IR, MS, ¹H and ¹³C NMR, COSY and NOESY spectroscopy, X‐ray crystallographic analysis, and by comparison with the authentic sample prepared with the known procedure. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:694–699, 2008; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20497     

Iodo cyclofunctionalization of 2,4‐dialkenyl‐1,3‐dicarbonyl compounds: Synthesis of substituted 3‐(2‐furylidene)‐2‐furanones

A facile method for the synthesis of substituted 3‐(2‐furylidene)‐2‐furanones has been developed using cyclofunctionalization reactions of 2,4‐dialkenyl‐1,3‐dicarbonyl compounds and iodine as electrophile in the presence of Na₂CO₃, in refluxing chloroform. Compounds 4 are obtained in modest to good yields and their structural identification was established by ¹H NMR, ¹H COSY, ¹³C NMR and ¹H‐¹³C COSY. A mechanism has been proposed to rationalize the formation of the ylidene furanone.     

Isolation and Structural Characterization of New,Highly Functionalized Diterpenes from Euphorbia serrulata

Five new diterpene polyesters, 1 – 5 , with jatrophane skeletons were isolated from the fresh whole plants of Euphorbia serrulata. The structure elucidation was performed by means of UV/VIS spectroscopy, HR‐ESI‐MS, and advanced two‐dimensional NMR methods, including ¹H‐NMR, JMOD, ¹H,¹H‐COSY, NOESY, HMQC, and HMBC experiments. The relative configurations of 1 – 5 and their conformations in solution were analyzed on the basis of NOESY measurements. As a result of detailed NMR studies, complete ¹H and ¹³C chemical‐shift assignments of the compounds were possible. The isolated compounds differ stereochemically and do not comprise a uniform series regarding the configurations at C(2), C(6), and C(13). Compound 5 possesses the new structural feature of a double bond with (Z)‐configuration in the macrocyclic ring of the jatrophane skeleton, while compound 2 has a C?C bond in the five‐membered ring, this being the first observation of this structural feature in the type of macrocyclic Euphorbiaceae diterpenes.     

Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek

The triterpene ester (3β)‐olean‐18‐en‐3‐yl stearate ( 1 ), together with (3β)‐urs‐12‐en‐3‐yl stearate ( 2 ), and (3β)‐lup‐20(29)‐en‐3‐yl stearate ( 3 ) were isolated from leaves of Maytenus salicifolia Reissek (Celastraceae). The structure of 1 , a new compound, including its configuration, was established by ¹H, ¹³C, and DEPT‐135 NMR data, including 2D experiments (HSQC, HMBC, COSY, and NOESY). The molecular mass (692 Da) was confirmed by gas chromatography coupled with mass spectrometry (CG/MS).     

Synthesis and NMR characteristics of N‐acetyl‐4‐nitro,N‐acetyl‐5‐nitro,N‐acetyl‐6‐nitro and N‐acetyl‐7‐nitrotryptophan methyl esters

N‐acetyl‐4‐nitrotryptophan methyl ester (2), N‐acetyl‐5‐nitrotryptophan methyl ester (3), N‐acetyl‐6‐nitrotryptophan methyl ester (4) and N‐acetyl‐7‐nitrotryptophan methyl ester (5) were synthesized through a modified malonic ester reaction of the appropriate nitrogramine analogs followed by methylation with BF₃‐methanol. Assignments of the ¹H and ¹³C NMR chemical shifts were made using a combination of ¹H–¹H COSY, ¹H–¹³C HETCOR and ¹H–¹³C selective INEPT experiments. Copyright © 2008 Crown in the right of Canada. Published by John Wiley & Sons, Ltd     

Systematical NMR analysis of swainsonine,a mycotoxin from endophytic fungus Alternaria oxytropis

Swainsonine (SW, 1 ), a unique indolizine with poly‐hydroxyl groups, was re‐isolated from the plant endophytic fungus Alternaria oxytropis. The structure (including planar structure and relative configuration) was systematically elucidated by NMR spectra (including ¹H, ¹³C, ¹H‐¹H COSY, HMQC, HMBC, and NOESY spectra in DMSO‐d₆ and in CD₃OD); ¹H NMR spectra of the modified Mosher's products were first used to determine the absolute configuration of SW. More importantly, the complex coupled features of H‐7α, H‐7β, and H‐6α in the ¹H NMR spectrum of ( 1 ) were analyzed in details, which will provide aids for the planar and relative configuration determination of analogs.