(Q38940745)

7 September 2017

Total synthesis, stereochemical reassignment, and biological evaluation of (-)-lyngbyaloside B. (English)

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7 September 2017

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Haruhiko Fuwa

1

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author name string

Yuta Okuaki

series ordinal

2

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7 September 2017

Naoya Yamagata

series ordinal

3

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7 September 2017

Makoto Sasaki

series ordinal

4

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7 September 2017

language of work or name

English

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publication date

12 November 2014

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Angewandte Chemie International Edition

7 September 2017

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volume

54

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7 September 2017

3

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7 September 2017

868-873

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Mandelalides A-D, cytotoxic macrolides from a new Lissoclinum species of South African tunicate

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Cytotoxic halogenated macrolides and modified peptides from the apratoxin-producing marine cyanobacterium Lyngbya bouillonii from Guam

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Lyngbouilloside, a novel glycosidic macrolide from the marine cyanobacterium Lyngbya bouillonii

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Dual macrolactonization/pyran-hemiketal formation via acylketenes: applications to the synthesis of (-)-callipeltoside A and a lyngbyaloside B model system

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Stereoselective synthesis of the C9-C19 fragment of lyngbyaloside B and C via ether transfer

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Total synthesis of 13-demethyllyngbyaloside B.

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The Liebeskind-Srogl C-C cross-coupling reaction.

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Bond formations by intermolecular and intramolecular trappings of acylketenes and their applications in natural product synthesis.

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Boron-mediated aldol reaction of carboxylic esters: complementary anti- and syn-selective asymmetric aldol reactions

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Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragment

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Stereocontrolled total synthesis of the Stemona alkaloid (-)-stenine

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Oxidation of α,β-un saturated aldehydes

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Total synthesis of (-)-callipeltoside A

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Total synthesis of (+)-A83543A [(+)-lepicidin A]

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Total synthesis and biological evaluation of (+)-neopeltolide and its analogues

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Modular total synthesis of rhizopodin: a highly potent G-actin dimerizing macrolide.

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A general, asymmetric, and noniterative synthesis of trideoxypropionates. Straightforward syntheses of the pheromones (+)-vittatalactone and (+)-norvittatalactone

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Chasing molecules that were never there: misassigned natural products and the role of chemical synthesis in modern structure elucidation

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Structural revisions of natural products by total synthesis

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Recent synthetic studies leading to structural revisions of marine natural products

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Survey of marine natural product structure revisions: a synergy of spectroscopy and chemical synthesis

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Total synthesis, structure revision, and absolute configuration of (-)-brevenal

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Total synthesis and structure revision of didemnaketal B.

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Einfache Synthese von α-und β-O-Glykosylimidaten; Herstellung von Glykosiden und Disacchariden

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Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide

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Simple and selective method for aldehydes (RCHO) .fwdarw. (E)-haloalkenes (RCH:CHX) conversion by means of a haloform-chromous chloride system

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Total Synthesis and Complete Stereostructure of Gambieric Acid A

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Aurisides A and B, Cytotoxic Macrolide Glycosides from the Japanese Sea HareDolabella auricularia

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Divergent total synthesis of the antimitotic agent leiodermatolide

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Total Synthesis of Bafilomycin A1

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Lyngbyaloside B, a new glycoside macrolide from a Palauan marine cyanobacterium, Lyngbya sp

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Callipeltoside A: A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida SpongeCallipeltasp

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Boron-mediated aldol reaction of carboxylic esters

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Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes

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Polycavernoside A: a novel glycosidic macrolide from the red alga Polycavernosa tsudai (Gracilaria edulis)

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Total Synthesis of Nominal Lyngbouilloside Aglycon

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Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones

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A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species

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Convergent and enantioselective total synthesis of (-)-amphidinolide O and (-)-amphidinolide P

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Identifiers

DOI

10.1002/ANIE.201409629

1 reference

7 September 2017

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