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Preparation of chiral C5-building blocks for terpene synthesis by bakers' yeast reduction of sulfur-functionalized prenyl derivatives
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20/20 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
6 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 20 checked references that resolve
resolves10.1002/anie.198405701
Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]
resolves10.1002/hlca.19790620210
Totalsynthese von natürlichem α‐Tocopherol. 1. Mitteilung. Herstellung bifunktioneller, optisch aktiver Synthesebausteine für die Seitenkette mit Hilfe mikrobiologischer Umwandlungen
resolves10.1021/jo00223a038
Chiral synthetic intermediates via asymmetric hydrogenation of .alpha.-methyl-.alpha.,.beta.-unsaturated aldehydes by bakers' yeast
resolves10.1246/cl.1983.237
ASYMMETRICAL REDUCTION OF PERFLUOROALKYLATED KETONES, KETOESTERS AND VINYL COMPOUNDS WITH BAKER’S YEAST
resolves10.1246/cl.1987.971
Asymmetric Reduction of α-Methylene Ketones by Using Fermenting Baker’s Yeast. Preparation of Optically Active β-Hydroxy α-Methyl Ketones
resolves10.1007/BF01972264
Stereospecific reduction of geraniol to (R)-(+)-citronellol bySaccharomyces cerevisiae
resolves10.1246/cl.1987.191
Asymmetric Hydrogenation of 2-Aryl-1-nitropropenes by Fermenting Bakers’ Yeast
resolves10.1016/S0040-4039(01)91125-6
Enantiospecific synthesis of optically pure (3s)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters
resolves10.1016/S0040-4039(00)89133-9
Optically pure (s)-3-phenylthio-1,2-propanediol: synthesis by the yeast reduction and use as a precursor of both enantiomers of secondary alcohols
resolves10.1246/cl.1985.1679
A SIMPLE STEREOCONTROLLED SYNTHESES OF OPTICALLY ACTIVE DEOXYSUGARS <scp>l</scp>-RHODINOSE AND <scp>d</scp>-AMICETOSE
resolves10.1246/cl.1985.1751
ENANTIOSELECTIVE SYNTHESIS OF α-HYDROXYTHIOACETALS BY THE BAKER’S YEAST REDUCTION OF α-KETOTHIOACETALS
resolves10.1016/S0040-4039(00)95133-5
Diastereo- and enantioselective reduction of α,β-diketodithiane with the baker's yeast
resolves10.1246/cl.1987.2227
(2<i>S</i>,3<i>S</i>)-1-Phenylthio-2,3-butanediol. A Useful Chiral Building Block for a Simple Syntheses of (4<i>R</i>,5<i>S</i>)-5-Hydroxyhexan-4-olide and (4<i>R</i>,5<i>S</i>)-5-Hydroxy-2-hexen-4-olide
resolves10.1021/jo00981a013
Synthesis and properties of 2-(2-cyanoethylidene)-1,3-dithiane and its isomeric ketene thioacetal
resolves10.1246/cl.1977.39
ALICYCLIC TERPENOIDS FROM CYCLOCITRYL PHENYL SULFIDES. IV. A SYNTHESIS OF METHYL ESTERS OF VITAMIN A1 AND A2 ACIDS AND THEIR GEOMETRIC ISOMERS
resolves10.1021/ja01166a076
The Reaction of Isoprene with t-Butyl Hypochlorite in Hydroxylic Solvents
resolves10.1021/ja00346a035
Palladium-mediated cycloaddition approach to cyclopentanoids. Introduction and initial studies
resolves10.1055/s-1979-28713
Allylsilanes in Organic Synthesis: A Method for the Introduction of Two Carbon Substituents in Place of Carbonyl Oxygen
The 6 references without a DOI — listed, not checked
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib1
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib4.A
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib7
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib10.F
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib14
no DOI — not checked10.1016/S0040-4039(00)86710-6_bib16
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