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Total Synthesis of (+)-Calyculin A and (−)-Calyculin B: Asymmetric Synthesis of the C(9−25) Spiroketal Dipropionate Subunit

https://doi.org/10.1021/ja992134m
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.199406731openalex-snapshot
The Synthesis of Naturally Occurring ()‐Calyculin A
inferredcites →https://doi.org/10.1002/hlca.19820650141openalex-snapshot
Substitution of HMPT by the cyclic urea DMPU as a cosolvent for highly reactive nucleophiles and bases
inferredcites →https://doi.org/10.1002/hlca.19840670421openalex-snapshot
Low‐Temperature 13C‐NMR Spectra of 6Li‐ and 13C‐Labelled Sulfur‐ and Selenium‐Substituted Organolithium Derivatives
inferredcites →https://doi.org/10.1002/mc.2940020403openalex-snapshot
Codon 61 Mutations in the c‐Harvey‐ras Gene in Mouse Skin Tumors Induced by 7,12‐Dimethylbenz[a]anthracene Plus Okadaic Acid Class Tumor Promoters
inferredcites →https://doi.org/10.1016/0006-291x(89)92189-xopenalex-snapshot
Calyculin A and okadaic acid: Inhibitors of protein phosphatase activity
inferredcites →https://doi.org/10.1016/0022-328x(85)87388-5openalex-snapshot
More highly mixed, higher order cyanocuprates “RT(2-thienyl)Cu(CN)Li2”. Efficient reagents which promote selective ligand transfer
inferredcites →https://doi.org/10.1016/0040-4020(84)80005-8openalex-snapshot
Stereoselective acyclic ketone reduction
inferredcites →https://doi.org/10.1016/0040-4039(91)80096-oopenalex-snapshot
Absolute Stereochemistry of the Calyculins, Potent Inhibitors of Protein Phosphatases 1 and 2A
inferredcites →https://doi.org/10.1016/0040-4039(91)80459-jopenalex-snapshot
Enantiospecific synthesis of polyhydroxy amino acids. Synthesis of the C33C38 portion of calyculins.
inferredcites →https://doi.org/10.1016/0040-4039(92)88107-gopenalex-snapshot
Towards the Synthesis of Calyculin: A Synthetic Intermediate Corresponding to the C(26)-C(37) Fragment
inferredcites →https://doi.org/10.1016/0040-4039(94)88072-7openalex-snapshot
Calyculin synthetic studies. 4. remarkable reversal of diastereo-selectivity in payne epoxidation of vinyl spiroketal intermediates
inferredcites →https://doi.org/10.1016/0040-4039(95)00274-gopenalex-snapshot
A caveat on the Sharpless asymmetric dihydroxylation
inferredcites →https://doi.org/10.1016/0968-0004(90)90192-eopenalex-snapshot
Okadaic acid: a new probe for the study of cellular regulation
inferredcites →https://doi.org/10.1016/s0022-3565(25)21393-3openalex-snapshot
Calcium-independent activation of contractile apparatus in smooth muscle by calyculin-A.
inferredcites →https://doi.org/10.1016/s0040-4020(01)83440-2openalex-snapshot
Tremorgenic indole alkaloid studies. 6. Preparation of an advanced intermediate for the synthesis of penitrem D. Synthesis of an indole oxocane
inferredcites →https://doi.org/10.1016/s0040-4020(01)91961-1openalex-snapshot
Recent advances in the preparation and synthetic applications of oxiranes
inferredcites →https://doi.org/10.1016/s0040-4020(01)92726-7openalex-snapshot
A simplified procedure for epoxidation by benzonitrile-hydrogen peroxide. Selective oxidation of 2-allylcyclohexanone
inferredcites →https://doi.org/10.1016/s0040-4020(01)96031-4openalex-snapshot
Calyculins E, F, G, and H, additional inhibitors of protein phosphatases 1 and 2a, from the marine sponge discodermia calyx
inferredcites →https://doi.org/10.1016/s0040-4039(00)61904-4openalex-snapshot
Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides
inferredcites →https://doi.org/10.1016/s0040-4039(00)70661-7openalex-snapshot
Synthetic study on aplysiatoxins, highly inflammatory agents and tumor promoters synthesis of 3-deoxydebromoaplysiatoxin
inferredcites →https://doi.org/10.1016/s0040-4039(00)74284-5openalex-snapshot
Synthesis of trans-4-alkenyl oxazoles
inferredcites →https://doi.org/10.1016/s0040-4039(00)74685-5openalex-snapshot
A synthesis of the tetraene fragment of calyculins as its antipodal form
inferredcites →https://doi.org/10.1016/s0040-4039(00)76209-5openalex-snapshot
Calyculin synthetic studies. 3. Enantiomeric purity determination for the C(26)–C(32) oxazole segment via the silks-odom 77Se NMR method
inferredcites →https://doi.org/10.1016/s0040-4039(00)76920-6openalex-snapshot
Towards the synthesis of swinholide A and scytophycin C. A highly stereocontrolled synthesis of (−)-pre-swinholide A
inferredcites →https://doi.org/10.1016/s0040-4039(00)78251-7openalex-snapshot
Regiochemistry of wacker-type oxidation of vinyl group in the presence of neighboring oxygen functions
inferredcites →https://doi.org/10.1016/s0040-4039(00)79009-5openalex-snapshot
Iodine monobromide (IBr) at low temperature: A superior protocol for diastereoselective cyclizations of homoallylic carbonates
inferredcites →https://doi.org/10.1016/s0040-4039(00)79444-5openalex-snapshot
Stereoselective Synthesis of 2,3-dihydroxy-4-dimethylamino-5-methoxypentanoic acid, a fragment of calyculins ------- determination of the absolute configuration of calyculins
inferredcites →https://doi.org/10.1016/s0040-4039(00)80611-5openalex-snapshot
An examination of the coupling of vinyl and aryl triflates with stannyl cuprates for the purpose of providing regioselective access to vinyl lithiums
inferredcites →https://doi.org/10.1016/s0040-4039(00)81581-6openalex-snapshot
A method for the regiospecific synthesis of enol triflates by enolate trapping
inferredcites →https://doi.org/10.1016/s0040-4039(00)84071-xopenalex-snapshot
Convenient access to two enantiomeric oxirane synthons bearing a quaternary gem-dimethyl carbon center: Synthesis of 3S-(+) and 3R-(−)-2,2-dimethyl-3,4-oxo-1-butanol from R-(−)-pantolactone
inferredcites →https://doi.org/10.1016/s0040-4039(00)88071-5openalex-snapshot
Cleavage of carbonoxygen bonds. Dimethylboron bromide. A new reagent for ether cleavage
inferredcites →https://doi.org/10.1016/s0040-4039(00)88238-6openalex-snapshot
Dimethylboron bromide and diphenylboron bromide. Acetal and ketal cleavage. Cleavage of MEM, MOM, and MTM ethers.
inferredcites →https://doi.org/10.1016/s0040-4039(00)93479-8openalex-snapshot
Calyculin synthetic studies. Stereoselective construction of the C(14)-C(25) spiroketal subunit
inferredcites →https://doi.org/10.1016/s0040-4039(00)93480-4openalex-snapshot
Calyculin synthetic studies. 2. Stereocontrolled assembly of the C(9)-C(13) dithiane and C(26)-C(37) oxazole intermediates
inferredcites →https://doi.org/10.1016/s0040-4039(00)94399-5openalex-snapshot
Stereochemistry of alternating polyol chains: 13C NMR analysis of 1,3-diol acetonides
inferredcites →https://doi.org/10.1016/s0040-4039(00)97005-9openalex-snapshot
Reversal of aldehyde diastereofacial selectivity in a methyl ketone aldol reaction. Application to the synthesis of the calyculin spiroketal
inferredcites →https://doi.org/10.1016/s0040-4039(00)97250-2openalex-snapshot
13C NMR chemical shift correlations in 1,3-diol acetonides. Implications for the stereochemical assignment of propionate-derived polyols
inferredcites →https://doi.org/10.1016/s0040-4039(01)80310-5openalex-snapshot
Progress toward roflamycoin; Synthesis of the C-12 to C-35 section in homochiral form
inferredcites →https://doi.org/10.1016/s0040-4039(01)85590-8openalex-snapshot
Synthesis of antisecretory prostaglandins using vinyl tin precursors
inferredcites →https://doi.org/10.1016/s0040-4039(01)94849-xopenalex-snapshot
Synthetic studies on polyether antibiotics. II. Stereocontrolled syntheses of epoxides of bishomoallylic alcohols.
inferredcites →https://doi.org/10.1016/s0040-4039(97)00748-xopenalex-snapshot
Isolation of dephosphonocalyculin a from the marine sponge, Discodermia calyx
inferredcites →https://doi.org/10.1016/s0040-4039(98)01992-3openalex-snapshot
Convenient Wacker oxidations with substoichiometric cupric acetate
inferredcites →https://doi.org/10.1016/s0040-4039(99)00222-1openalex-snapshot
Remarkable long range effects on the diastereoface selectivity in an aldol condensation
inferredcites →https://doi.org/10.1016/s0968-0896(97)00146-6openalex-snapshot
Inhibition of the ser-thr phosphatases PP1 and PP2A by naturally occurring toxins
inferredcites →https://doi.org/10.1021/ar960289iopenalex-snapshot
Total Synthesis of Immunosuppressants: Unified Strategies Exploiting Dithiane Couplings and σ-Bond Olefin Constructions
inferredcites →https://doi.org/10.1021/cen-v027n009.p590openalex-snapshot
115th National Meeting American Chemical Society
inferredcites →https://doi.org/10.1021/cen-v036n010.p076openalex-snapshot
The 133rd NATIONAL MEETING AMERICAN CHEMICAL SOCIETY
inferredcites →https://doi.org/10.1021/cr00032a009openalex-snapshot
Catalytic Asymmetric Dihydroxylation
inferredcites →https://doi.org/10.1021/ja00050a024openalex-snapshot
Total synthesis of (+)-calyculin A
inferredcites →https://doi.org/10.1021/ja00173a024openalex-snapshot
Acyclic diastereoselective synthesis using tartrate ester-modified crotylboronates. Double asymmetric reactions with .alpha.-methyl chiral aldehydes and synthesis of the C(19)-C(29) segment of rifamycin S
inferredcites →https://doi.org/10.1021/ja00213a029openalex-snapshot
Chiral synthesis via organoboranes. 13. A highly diastereoselective and enantioselective addition of [(Z)-.gamma.-alkoxyallyl]diisopinocampheylboranes to aldehydes
inferredcites →https://doi.org/10.1021/ja00216a045openalex-snapshot
In situ cuprate formation via transmetalation between vinylstannanes and higher order cyanocuprates
inferredcites →https://doi.org/10.1021/ja00254a062openalex-snapshot
Total synthesis of debromoaplysiatoxin and aplysiatoxin
inferredcites →https://doi.org/10.1021/ja00262a017openalex-snapshot
Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcohols
inferredcites →https://doi.org/10.1021/ja00270a061openalex-snapshot
Bioactive marine metabolites. Part 16. Calyculin A. A novel antitumor metabolite from the marine sponge Discodermia calyx
inferredcites →https://doi.org/10.1021/ja00279a042openalex-snapshot
Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes
inferredcites →https://doi.org/10.1021/ja00330a045openalex-snapshot
Enantiodivergent syntheses of (+)- and (-)-nonactic acid and the total synthesis of nonactin
inferredcites →https://doi.org/10.1021/ja00388a074openalex-snapshot
Total synthesis of aplasmomycin
inferredcites →https://doi.org/10.1021/ja00415a067openalex-snapshot
Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state model
inferredcites →https://doi.org/10.1021/ja00457a020openalex-snapshot
Thiosilanes, a promising class of reagents for selective carbonyl protection
inferredcites →https://doi.org/10.1021/ja00775a089openalex-snapshot
Mixed cuprate reagents of type R1R2CuLi which allow selective group transfer
inferredcites →https://doi.org/10.1021/ja00801a066openalex-snapshot
Novel synthesis of prostaglandin F2.alpha.
inferredcites →https://doi.org/10.1021/ja00997a067openalex-snapshot
Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide
inferredcites →https://doi.org/10.1021/ja01092a068openalex-snapshot
Alkyllithium-Amine Crystalline Complexes
inferredcites →https://doi.org/10.1021/ja962559yopenalex-snapshot
β-Silyl Organocuprates: The Grail of Organocuprate Chemistry? 1 a
inferredcites →https://doi.org/10.1021/ja963066wopenalex-snapshot
A Unified Total Synthesis of the Immunomodulators (−)-Rapamycin and (−)-27-Demethoxyrapamycin: Construction of the C(21−42) Perimeters
inferredcites →https://doi.org/10.1021/ja980836qopenalex-snapshot
Total Synthesis of Calyculin C
inferredcites →https://doi.org/10.1021/jo00033a009openalex-snapshot
Asymmetric synthesis of calyculin A. 1. The C1-C25 spiroketal fragment
inferredcites →https://doi.org/10.1021/jo00033a010openalex-snapshot
Asymmetric synthesis of calyculin A. 2. The C26-C37 .gamma.-amino acid fragments
inferredcites →https://doi.org/10.1021/jo00033a011openalex-snapshot
Asymmetric synthesis of calyculin A. 3. Assemblage of the calyculin skeleton and the introduction of a new phosphate monoester synthesis
inferredcites →https://doi.org/10.1021/jo00066a024openalex-snapshot
Iodine monobromide (IBr) at low temperature: enhanced diastereoselectivity in electrophilic cyclizations of homoallylic carbonates
inferredcites →https://doi.org/10.1021/jo00142a002openalex-snapshot
Carbonate extension. A versatile procedure for functionalization of acyclic homoallylic alcohols with moderate stereocontrol
inferredcites →https://doi.org/10.1021/jo00187a001openalex-snapshot
Intramolecular nitrile oxide cycloaddition route to carbocyclics: a formal total synthesis of PGF2.alpha.
inferredcites →https://doi.org/10.1021/jo00252a009openalex-snapshot
Bioactive marine metabolites. 24. Isolation and structure elucidation of calyculins B, C, and D, novel antitumor metabolites, from the marine sponge Discodermia calyx
inferredcites →https://doi.org/10.1021/jo00257a035openalex-snapshot
Dilithium (trimethylstannyl)(2-thienyl)(cyano)cuprate, a synthetically useful higher-order cuprate reagent
inferredcites →https://doi.org/10.1021/jo00362a036openalex-snapshot
On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols
inferredcites →https://doi.org/10.1021/jo00392a036openalex-snapshot
Electrophilic destannylation: stereospecific introduction of electrophiles at the 21 position of (17.alpha.)-19-norpregna-1,3,5(10),20-tetraene-3,17.beta.-diols
inferredcites →https://doi.org/10.1021/jo00900a022openalex-snapshot
Mild and convenient oxidation procedure for the conversion of organoboranes to the corresponding alcohols
inferredcites →https://doi.org/10.1021/jo01280a018openalex-snapshot
Stereochemistry of epoxidation of rigid methylenecyclohexane systems. Determination of stereochemistry of exocyclic epoxides in rigid cyclohexanes by nuclear magnetic resonance half band widths
inferredcites →https://doi.org/10.1021/jo960315qopenalex-snapshot
Asymmetric Synthesis of Calyculin C. 2. Synthesis of the C26−C37 Fragment and Model Wittig Couplings
inferredcites →https://doi.org/10.1021/jo961745jopenalex-snapshot
Isolation of Calyculins, Calyculinamides, and Swinholide H from the New Zealand Deep-Water Marine Sponge Lamellomorpha strongylata
inferredcites →https://doi.org/10.1021/jo971167mopenalex-snapshot
Synthesis of the C26−C32 Oxazole Fragment of Calyculin C: A Test Case for Oxazole Syntheses
inferredcites →https://doi.org/10.1021/jo981813xopenalex-snapshot
Total Synthesis of (+)-Calyculin A and (−)-Calyculin B
inferredcites →https://doi.org/10.1039/c39920001236openalex-snapshot
Stereocontrolled synthesis of calyculin A: construction of the C(15)–C(25) spiroketal unit
inferredcites →https://doi.org/10.1039/c39920001238openalex-snapshot
Stereocontrolled synthesis of calyculin A: construction of the C(1)–C(14) tetraene nitrile unit
inferredcites →https://doi.org/10.1039/c39920001240openalex-snapshot
Stereocontrolled synthesis of calyculin A: construction of the C(26)–C(37) amide-oxazole unit
inferredcites →https://doi.org/10.1039/ct9150701080openalex-snapshot
CXIX.—The formation and stability of spiro-compounds. Part I. spiro-Compounds from cyclohexane
inferredcites →https://doi.org/10.1039/p19810001317openalex-snapshot
Enantio-complementary total asymmetric syntheses of prostaglandin E2 and prostaglandin F2?
inferredcites →https://doi.org/10.1039/p19940001901openalex-snapshot
Synthetic studies on calyculin a: a convenient asymmetric synthesis of anti-vicinal diols
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Activated Dimethyl Sulfoxide: Useful Reagents for Synthesis
inferredcites →https://doi.org/10.1055/s-1984-30848openalex-snapshot
Synthetic Applications of the Palladium-Catalyzed Oxidation of Olefins to Ketones
inferredcites →https://doi.org/10.1055/s-1990-27036openalex-snapshot
Oxidation of Alcohols by Activated Dimethyl Sulfoxide and Related Reactions: An Update
inferredcites →https://doi.org/10.1055/s-1991-20709openalex-snapshot
Stereoselective Synthesis of the C13-C19 Fragment of the Cytotoxic Marine Products Calyculins; Part 11
inferredcites →https://doi.org/10.1055/s-1991-20710openalex-snapshot
Stereoselective Synthesis of the C13-C19 Fragment of the Cytotoxic Marine Products Calyculins; Part 21
inferredcites →https://doi.org/10.1055/s-1992-21297openalex-snapshot
A Synthesis of the Oxazole Part of Calyculins; Part 1
inferredcites →https://doi.org/10.1055/s-1992-21298openalex-snapshot
A Synthesis of the Oxazole Part of Calyculins; Part 2
inferredcites →https://doi.org/10.1080/00397919608003698openalex-snapshot
A Practical Asymmetric Synthesis of A Pseudomonic Acid Precursor from D-Arabinose or D-Xylose
inferredcites →https://doi.org/10.1246/cl.1983.1593openalex-snapshot
A FACILE CLEAVAGE OF BENZYLIDENE ACETALS WITH DIISOBUTYLALUMINUM HYDRIDE
inferredcites →https://doi.org/10.1248/cpb.34.3102openalex-snapshot
Synthesis of a new amino acid-antibiotic, oxetin and its three stereoisomers.
inferredcites →https://doi.org/10.1351/pac199163020283openalex-snapshot
Models for selectivity in organic reactions
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Base-assisted Migration of Trimethylsilyl Group from Carbon to Oxygen in g-Trimethylsilyl-g,d-unsaturated Alcohols, g-Trimethylsilyl-g,d-epoxy Alcohols, and b-Trimethylsilyl-b,g-epoxy Alcohols to the Corresponding Silyl Ethers

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Iodine Monobromide
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Iodine Monobromide
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B-(Z)-γ-Methoxyallyldiisopinocampheylborane
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Allylboration of Carbonyl Compounds
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Wacker Oxidation, The
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Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols
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Protection for the Amino Group
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Roush Crotylboration
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Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols
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Protection for the Amino Group
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Porifera (Sponges)–5
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Wacker oxidation
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Wacker Oxidation
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Wacker oxidation
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Wacker oxidation
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Synthesis and in vitro evaluation of analogues of avocado-produced toxin (+)-(R)-persin in human breast cancer cells
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An expedient synthesis of spiroketals: model studies for the calyculin C16–C25 fragment
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Substrate stereocontrol in bromine-induced intermolecular cyclization: asymmetric synthesis of pitavastatin calcium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.181openalex-snapshot
Synthesis of the C1–C12 fragment of the tedanolides. Selective hydroboration–protonation of allylic alcohol approach
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.030openalex-snapshot
Complementary α-alkylation approaches for a sterically hindered spiro[pyrazolopyranpiperidine]ketone
inferred← citeshttps://doi.org/10.1016/s0010-8545(01)00401-5openalex-snapshot
Transition metals in organic synthesis: highlights for the year 1999
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00474-4openalex-snapshot
Increase in intricacy—a tool for evaluating organic syntheses
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00059-5openalex-snapshot
A convergent synthesis of the spiroketal moiety of the HIV-1 protease inhibitors didemnaketals
inferred← citeshttps://doi.org/10.1016/s0040-4020(03)00955-4openalex-snapshot
The role of 1,3-dithianes in natural product synthesis
inferred← citeshttps://doi.org/10.1021/cc010047wopenalex-snapshot
Combinatorial Synthesis of Natural Product-like Molecules Using a First-Generation Spiroketal Scaffold
inferred← citeshttps://doi.org/10.1021/cr0509915openalex-snapshot
Alkynylation of Chiral Aldehydes: Alkoxy-, Amino-, and Thio-Substituted Aldehydes
inferred← citeshttps://doi.org/10.1021/ja020635topenalex-snapshot
Total Syntheses of (+)-Zampanolide and (+)-Dactylolide Exploiting a Unified Strategy
inferred← citeshttps://doi.org/10.1021/ja0376238openalex-snapshot
Multicomponent Linchpin Couplings. Reaction of Dithiane Anions with Terminal Epoxides, Epichlorohydrin, and Vinyl Epoxides: Efficient, Rapid, and Stereocontrolled Assembly of Advanced Fragments for Complex Molecule Synthesis
inferred← citeshttps://doi.org/10.1021/ja1016975openalex-snapshot
Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon
inferred← citeshttps://doi.org/10.1021/jo0056951openalex-snapshot
Synthesis of a C1−C21 Subunit of the Protein Phosphatase Inhibitor Tautomycin: A Formal Total Synthesis
inferred← citeshttps://doi.org/10.1021/jo201729topenalex-snapshot
Synthesis of the Bis-Spiroacetal Core of the Antimitotic Agent Spirastrellolide B
inferred← citeshttps://doi.org/10.1021/jo402167qopenalex-snapshot
NH4HF2 as a Selective TBS-Removal Reagent for the Synthesis of Highly Functionalized Spiroketal via Tandem Deprotection/Spiroketalization Procedure
inferred← citeshttps://doi.org/10.1021/jo801106bopenalex-snapshot
Diastereoselective Synthesis of Useful Building Blocks by Crotylation of β-Branched α-Methylaldehydes with Potassium Crotyltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol005634popenalex-snapshot
Chiral Action at a Distance: Remote Substituent Effects on the Optical Activity of Calyculins A and B
inferred← citeshttps://doi.org/10.1021/ol027095popenalex-snapshot
SmI2-Promoted Oxidation of Aldehydes in the Presence of Electron-Rich Heteroatoms
inferred← citeshttps://doi.org/10.1021/ol047792copenalex-snapshot
Diversity-Oriented Synthesis of Polyketide Natural Products via Iterative Chemo- and Stereoselective Functionalization of Polyenoates: Development of a Unified Approach for the C(1−19) Segments of Lituarines A−C
inferred← citeshttps://doi.org/10.1021/ol053115mopenalex-snapshot
Total Synthesis and Stereochemical Assignment of the Spiroisoxazoline Natural Product (+)-Calafianin1
inferred← citeshttps://doi.org/10.1021/ol403566wopenalex-snapshot
Asymmetric Alcohol C–H Allylation and syn-Crotylation: C9–C20 of Tetrafibricin
inferred← citeshttps://doi.org/10.1021/ol701999hopenalex-snapshot
Asymmetric CuH-Catalyzed Hydrosilylations en Route to the C-9 Epimer of Amphidinoketide Ι
inferred← citeshttps://doi.org/10.1021/ol9021222openalex-snapshot
Synthesis of (S)-Jamaicamide C Carboxylic Acid
inferred← citeshttps://doi.org/10.1039/a907926bopenalex-snapshot
Stoichiometric asymmetric processes
inferred← citeshttps://doi.org/10.1039/b007064popenalex-snapshot
8 Synthesis highlights: a review of the literature for 1999
inferred← citeshttps://doi.org/10.1039/b007741kopenalex-snapshot
Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids
inferred← citeshttps://doi.org/10.1039/c0cc00056fopenalex-snapshot
Synthesis of the bis-spiroacetal C25–C40 moiety of the antimitotic agent spirastrellolide B using a bis-dithiane deprotection/spiroacetalisation sequence
inferred← citeshttps://doi.org/10.1039/c0ob00092bopenalex-snapshot
Towards the total synthesis of calyculin C: preparation of the C9–C25 spiroketal-dipropionate unit
inferred← citeshttps://doi.org/10.1039/c3ob41569dopenalex-snapshot
Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3
inferred← citeshttps://doi.org/10.1039/c4ob02136copenalex-snapshot
An enantioselective total synthesis of Sch-725674
inferred← citeshttps://doi.org/10.1039/c5np00123dopenalex-snapshot
Calyculin: Nature's way of making the sponge-derived cytotoxin
inferred← citeshttps://doi.org/10.1039/c7ob02127eopenalex-snapshot
Synthetic approaches to the C11–C27 fragments of bryostatins
inferred← citeshttps://doi.org/10.1039/d1np00078kopenalex-snapshot
The phosphate ester group in secondary metabolites
inferred← citeshttps://doi.org/10.3390/md80100122openalex-snapshot
Calyculins and Related Marine Natural Products as Serine- Threonine Protein Phosphatase PP1 and PP2A Inhibitors and Total Syntheses of Calyculin A, B, and C
inferred← citeshttps://doi.org/10.3987/com-08-s(n)11openalex-snapshot
Study of Synthetic Routes for the Spiroketal Fragment in Calyculin A Based on Conformational Analysis
inferred← citeshttps://doi.org/10.70675/054bc2a6z53ffz46aaza96fzd6afd9d3fef6openalex-snapshot
Le soufre en chimie des sucres : évaluation du potentiel synthétique pour la préparation de spiro-orthoesters et intérêt pour l'obtention d'analogues du C-KRN 7000
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