Y. Kameda, T. Mimuro, S. Kondo, T. Honda, and T.  Otomo
Structure of Ion Pair Receptor Combined with Li+Cl- in Concentrated Acetonitrile Solutions Studied by Neutron Diffraction with 6Li/7Li Isotopic Substitution Method
J. Phys. Chem. B, 128, 12533 (2024).
https://doi.org/10.1021/acs.jpcb.4c06139
 

​S. Kondo, T. Mimuro, A. Yoshida, R. Sugawara, and M. Hirasawa
Highly Concentrated Solution of Lithium Chloride in Organic Solvents with Heteroditopic Receptors
Chem. Lett., 53, upae198 (2024).
https://doi.org/10.1093/chemle/upae198
 

S. Kondo, Y. Yuki, H. Kumagai, Y. Yoshida, and C. Li
Anion recognition by phosphoric triamide-Based receptors
Bull. Chem. Soc. Jpn., 97, uoae085 (2024).
https://doi.org/10.1093/bulcsj/uoae085
 

M. Hirasawa, A. Orita, T. Mimuro, and S. Kondo
Unlocking the use of LiCl as an inexpensive salt for lithium-ion batteries with a novel anion receptor
Materials, 17, 3244 (2024).
https://doi.org/10.3390/ma17133244
 

K. Kurosawa, W. Kanomata, S. Konnno, G. Seong, S. Kondo, T. Naka, T. Adschiri, and T. Togashi
Relationship of the thermal decomposition temperature and formate ion structure in amine-copper formate complex: FTIR spectrum reveals the decomposition temperature of copper formate moiety
Mater. Trans., 65, 946 (2024).
http://doi.org/10.2320/matertrans.MT-N2024001
 

T. Mimuro, A. Yoshida, K. Kamo, M. Hirasawa, and S. Kondo
Highly soluble bisurea derivatives for anion recognition
Org. Biomol. Chem., 21, 5281 (2023).
https://doi.org/10.1039/D3OB00802A
 

S. Kondo, S. Abe, and H. Katagiri
Synthesis and photophysical properties of cyclosiloxanes with substituted naphthyl groups
Dyes Pigm., 217, 111394 (2023).
https://doi.org/10.1016/j.dyepig.2023.111394
 

S. Abe and S. Kondo
Fluorescene sensing of anions by silanediols bearing substituted naphthyl gruops
ChemPlusChem, 88, e202300006 (2023).
https://doi.org/10.1002/cplu.202300006
 

S. Kondo, M. Ito, H. Ogawa, W. Fujiwara, and H. Katagiri
Synthesis and characterization of cyclotri- and tetrasiloxanes with pyrenyl groups
ACS Omega, 7, 44398 (2022).
https://doi.org/10.1021/acsomega.2c06076
 

S. Kondo, N. Okada, S. Abe, R. Tanaka, M. Yamamura, and M. Unno
Anion recognition by silanetriol in acetonitrile
Org. Biomol. Chem., 20, 8925 (2022).
https://doi.org/10.1039/D2OB01596J
 

S. Kondo and J. Iioka
Isophthalamide bearing 1-pyrenylethynyl group as a highly fluorescent hydrogen bond motif for anion receptors
Tetrahedron Lett., 82, 153406 (2021).
https://doi.org/10.1016/j.tetlet.2021.153406
 

Y. Kayaba, K. Hojo, K. Ono, M. Shizaki, K. Kanaizuka, S. Kondo, M. Kurihara, M. Mitsuishi, and J. Matsui
Visible multi-color electrochromism by tailor-made color mixing at one electrode
Jpn. J. Appl. Phys., 59, 091006 (2020).
https://doi.org/10.35848/1347-4065/abb034
 

K. Osawa, H. Tagaya, and S. Kondo
Naked Eye Detection of Anions by 2,2’-Bianthracene Derivative Bearing Urea Groups in Various Organic Solvents
Chem. Lett., 49, 290-294 (2020).
https://doi.org/10.1246/cl.190924
 

K. Osawa, H. Tagaya, and S. Kondo
Induced circular dichroism of achiral cyclic bisurea via hydrogen bonds with chiral carboxylates
J. Org. Chem., 84, 6623-6630 (2019).
https://doi.org/10.1021/acs.joc.9b00073
 

J. W. Attard, K. Osawa, Y. Guan, J. Hatt, S. Kondo, A. Mattson
Silanediol anion binding and enantioselective catalysis
Synthesis, 51, 2107-2115 (2019).
https://doi.org/10.1055/s-0037-1612217
 

S. Kondo, Y. Nakadai, M. Unno
Recognition of dicarboxylates in aqueous acetonitrile by a dinuclear zinc(II) complex of 2,2'-binaphthalene-based receptor
Supramol. Chem., 31, 9-18 (2019).
https://doi.org/10.1080/10610278.2018.1522445
 

​Y. Kayaba, K. Hojyo, K. Ono, M. Ishizaki, K. Kanaizuka, S. Kondo, M. Kurihara, M. Mitsuishi, and J. Matsui
Electrochemical charge storage using layer-by-layer deposited film composed of redox polymer and inorganic nanoporticle
J. Photopolym. Sci. Technol., 31, 349-352 (2018).
https://doi.org/10.2494/photopolymer.31.349
 

S. Kondo, K. Sato, Y. Matsuta, and K. Osawa
Chiral recognition of anions by fluorescence tetraamide-based receptors bearing hydroxy groups from L-serine and L-threonine residues
Bull. Chem. Soc. Jpn., 91, 875-881 (2018).
https://doi.org/10.1246/bcsj.20180028
 

S. Kondo, K. Endo, J. Iioka, K. Sato, and Y. Matsuta
UV-vis and fluorescence detection by receptors based on an isophthalamide bearing a phenylethynyl group
Tetrahedron Lett., 58, 4115-4118 (2017).
https://doi.org/10.1016/j.tetlet.2017.09.043
 

A. Satake, Y. Ishizawa, H. Katagiri, and S. Kondo
Chloride selective macrocyclic bisurea derivatives with 2,2'-binaphthalene moieties as spacers
J. Org. Chem., 81, 9848-9857 (2016).
https://doi.org/10.1021/acs.joc.6b01959
 

A. M. Hardman-Baldwin, M. D. Visco, J. M. Wieting, C. Stern, S. Kondo, and A. E. Mattson
Silanediol-catalyzed chromenone functionalization
Org. Lett., 18, 3766-3769 (2016).
https://doi.org/10.1021/acs.orglett.6b01783
 

S. Kondo and Y. Matsuta
Ratiometric sensing of anions by tetraamide-based receptors bearing hydroxy groups from serine and threonine residues
Tetrahedron Lett., 57, 1113-1116 (2016).
https://doi.org/10.1016/j.tetlet.2016.01.097
 

S. Kondo, Y. Taguchi, and Y. Bie
Solvent dependent intramolecular excimer emission of di(1-pyrenyl)silane and di(1-pyrenyl)methane derivatives
RSC Adv., 5, 5846-5849 (2015).
https://doi.org/10.1039/c4ra12153h
 

S. Kondo, Y. Nakadai, and M. Unno
Pyrophosphate selective recognition by a Zn2+ complex of a 2,2'-binaphthalene derivative bearing di(2-pyridylmethyl)aminomethyl groups in aqueous solution
RSC Adv., 4, 27140-27145 (2014).
https://doi.org/10.1039/c4ra01941e
 

M. Yamamura, S. Kondo, and M. Unno
Ion pair recognition of ditopic receptor bearing silanol groups as anion recognition sites and a 2,2'-bipyridine moiety as a metal-coordination site
Tetrahedron Lett., 55, 646-649 (2014).
https://doi.org/10.1016/j.tetlet.2013.11.096
 

S. Kondo and R. Takai
Selective detection of dihydrogen phosphate anion by fluorescence change with tetraamide-based receptors bearing isoquinolyl and quinolyl moieties 
Org. Lett., 15, 538-541 (2013).
https://doi.org/10.1021/ol3033626
 

S. Kondo Y. Bie, and M. Yamamura
Ratiometric fluorescence detection of anions by silanediol-based receptors bearing anthryl and pyrenyl groups 
Org. Lett., 15, 520-523 (2013).
https://doi.org/10.1021/ol303332k
 

S. Kondo, N. Watanabe, F. Takahashi, N. Takeda, and M. Unno
Synthesis and photophysical properties of 2,2’-binaphthalene-based receptor bearing trimethylsilyl groups to improve the solubility 
J. Incl. Phenom. Macrocycl. Chem., 75, 31-38 (2013).
https://doi.org/10.1007/s10847-012-0142-8
 

Y. Mikata, T. Fujimoto, N. Imai, and S. Kondo
Differentiation of oxygen atom chirality in copper(II) complexes with dipicolylamine (DPA)-derived ligands 
Eur. J. Inorg. Chem., 4310-4317 (2012).
https://doi.org/10.1002/ejic.201200521
 

S. Kondo, S. Nakajima, and M. Unno
Ratiometric fluorescence detection of anions by an amide-based receptor bearing pyrenyl groups 
Bull. Chem. Soc. Jpn., 85, 698-700 (2012).
https://doi.org/10.1246/bcsj.20120054
 

S. Kondo, H. Sonoda, T. Katsu, and M. Unno
Improvement of solubility of 2,2'-binaphthalene derivatives bearing urea groups as anion receptors and their application to a chloride selective electrode 
Sens. Actuators B, 160, 684-690 (2011).
https://doi.org/10.1016/j.snb.2011.08.048
 

Y. Mikata, T. Fujimoto, T. Fujiwara, and S. Kondo
Intramolecular ether oxygen coordination in the zinc complexes with dipicolylamine (DPA)-derived ligands
Inorg. Chim. Acta, 370, 420-426 (2011).
https://doi.org/10.1016/j.ica.2011.02.022
 

S. Kondo, M. Nagamine, S. Karasawa, M. Ishihara, M. Unno, and Y. Yano
Anion recognition by 2,2'-binaphthalene derivatives bearing urea and thiourea groups at 8- and 8'-positions by UV-vis and fluorescence spectroscopies
Tetrahedron, 67, 943-950 (2011).
https://doi.org/10.1016/j.tet.2010.12.004
 

S. Kondo, T. Takahashi, Y. Takiguchi, and M. Unno
Synthesis and photophysical properties of a 2,2'-bianthracene-based receptor bearing two aza-15-crown-5 ethers for naked-eye detection of barium ion
Tetrahedron Lett., 52. 453-457 (2011).
https://doi.org/10.1016/j.tetlet.2010.11.091
 

S. Kondo
Anion recognition by 2,2'-binaphthalene bearing imidazolium groups in MeCN 
Supramol. Chem., 23, 29-36 (2011).
https://doi.org/10.1080/10610278.2010.506554
 

S. Kondo, Y. Kobayashi, and M. Unno
Anion recognition by D-ribose-based receptors
Tetrahedron Lett., 51, 2512-2514 (2010).
https://doi.org/10.1016/j.tetlet.2010.03.001
 

S. Kondo, N. Okada, R. Tanaka, M. Yamamura, and M. Unno
Anion recognition by 1,3-disiloxane-1,1,3,3-tetraols in organic solvents
Tetrahedron Lett., 50, 2754-2757 (2009).
https://doi.org/10.1016/j.tetlet.2009.03.134
 

H. Liu, S. Kondo, N. Takeda, and M. Unno
An efficient approach to monophneyl-functionalized octasissesquioxanes
Eur. J. Inorg. Chem., 1317-1319 (2009).
https://doi.org/10.1002/ejic.200900012
 

H. Liu, S. Kondo, N. Takeda, and M. Unno
Synthesis of octacarboxy spherosilicate
J. Am. Chem. Soc., 130, 10074-10074 (2008).
https://doi.org/10.1021/ja803513n
 

H. Liu, S. Kondo, R. Tanaka, H. Oku, and M. Unno
A spectroscopic investigation of incompletely condensed polyhedral oligomeric silsesquioxanes (POSS-mono-ol, POSS-diol and POSS-triol): Hydrogen-bonded interaction and host-guest complex
J. Organomet. Chem., 693, 1301-1308 (2008).
https://doi.org/10.1016/j.jorganchem.2008.01.027
 

S. Kondo, A. Fukuda, T. Yamamura, R. Tanaka, and M. Unno
Anion recognition by a disiloxane-1,3-diol in organic solvents
Tetrahedron Lett., 48, 7946-7949 (2007).
https://doi.org/10.1016/j.tetlet.2007.09.067
 

S. Kondo, T. Hayashi, Y. Sakuno, Y. Takezawa, M. Unno, and Y. Yano
Synthesis of cyclic bis- and trismelamine derivatives and their complexation properties with barbiturates
Org. Biomol. Chem., 5, 907-916 (2007).
[2007:249356] https://doi.org/10.1039/B615537E
 

S. Kondo, T. Harada, R. Tanaka, and M. Unno
Anion recognition by a silanediol-based receptor
Org. Lett., 8, 4621-4624 (2006).
[145:471584 2006:912248] https://doi.org/10.1021/ol061822p
 

S. Inokuma, M. Kuramami, S. Otsuki, T. Shirakawa, S. Kondo, Y. Nakamura, and J. Nishimura
Synthesis of crownophanes possessing bipydine moieties: bipydinocrownophanes exhibiting perfect extractability toward Ag+ ion
Tetrahedron, 62, 10005-10010 (2006).
[145:489213 2006:934754]https://doi.org/10.1016/j.tet.2006.08.005
 

S. Kondo and M. Sato
UV-vis and fluorescence spectroscopic detection of anions by the conformational restriction of 2,2'-binaphthalene derivatives bearing thiourea groups through a methylene spacer
Tetrahedron, 62, 4844-4850 (2006).
[145:75746]https://doi.org/10.1016/j.tet.2006.03.002
 

S. Kondo, T. Suzuki, T. Toyama, and Y. Yano
Anion recognition by 1,3-benzenedisulfonamide derivatives bearing phenolic hydroxyl groups in MeCN-d3
Bull. Chem. Soc. Jpn., 78, 1348-1350 (2005).
[143:52404]https://doi.org/10.1246/bcsj.78.1348
 

S. Kondo, T. Kinjo, and Y. Yano
Barium ion sensing by a 2,2'-binaphthalene derivative bearing two monoaza-15-crown-5 ethers
Tetrahedron Lett., 46, 3183-3186 (2005). 
[143:52404] https://doi.org/10.1016/j.tetlet.2005.03.054
 

S. Kondo, Y. Hiraoka, N. Kurumatani, and Y. Yano
Selective recognition of dihydrogen phosphate by receptors bearing pyridyl moieties as hydrogen bond acceptors
Chem. Commun., 1720-1722 (2005).
[142:481700] https://doi.org/10.1039/B417304J
 

S. Inokuma, H. Ide, T. Yonekura, T. Funaki, S. Kondo, S. Shiobara, T. Yoshihira, S. Tobita, and J. Nishimura
Synthesis and complexing properties of [2.n](2,6)pyridinocrownophanes
J. Org. Chem., 70, 1698-1703 (2005).
[2005:106898] https://doi.org/10.1021/jo0402374
 

S. Kondo, T. Kinjo, and Y. Yano
Synthesis of a novel intercalator based on 2,2'-binaphthalene bearing dimethylammonium groups
Bioorg. Med. Chem. Lett., 14, 1641-1643 (2004). 
[140:423460] https://doi.org/10.1016/j.bmcl.2004.01.061
 

S. Inokuma, T. Funaki, S. Kondo, and J. Nishimura
Complexing properties of two benzocrown-ether moieties arranged at a cyclobutane ring system
Tetrahedron, 60, 2043-2050 (2004).
[140:356851]https://doi.org/10.1016/j.tet.2003.12.064
 

S. Watanabe, N. Kosaka, S. Kondo, and Y. Yano
Flavin receptors. Effects of melamine derivatives bearing thiourea and thiouronium ion on the binding and reactivity of flavin mimics in chloroform
Bull. Chem. Soc. Jpn., 77, 569-574 (2004).
[141:6806]https://doi.org/10.1246/bcsj.77.569
 

S. Kondo, M. Nagamine, and Y. Yano
Synthesis and anion recognition properties of 8,8'-dithioureido-2,2'-binaphthalene
Tetrahedron Lett., 44, 8801-8804 (2003). 
[2003:867321]https://doi.org/10.1016/j.tetlet.2003.09.207
 

S. Watanabe, Y. Sakuno, S. Kondo, and Y. Yano
Recognition of nucleotides by melamine derivatives bearing a guanidinium ion through hydrogen bondings
Heterocycles, 60, 2217-2221 (2003).
[2003:867321] https://doi.org/10.3987/COM-03-9853
 

S. Inokuma, T. Sakaizawa, T. Funaki, T. Yonekura, H. Satoh, S. Kondo, Y. Nakamura, and J. Nishimura
Synthesis and complexing property of four-bridged crownopaddlanes
Tetrahedron, 59, 8183-8190 (2003).
[2003:746767]https://doi.org/10.1016/j.tet.2003.08.049
 

S. Kondo, T. Suzuki, and Y. Yano
Effect of hydroxyl group in receptors bearing disulfonamide on anion recognition in acetonitrile-d3
Tetrahedron Lett., 43, 7059-7061 (2002).
[138:136877]https://doi.org/10.1016/S0040-4039(02)01543-5
 

S. Kondo, Y. Sakuno, T. Yokoyama, and Y. Yano
Cooperative effect of a metal ion and hydrogen bonds on phosphodiester cleavage in acetonitrile
Chem. Lett., 830-831 (2001).
[135:344165]
 

H. Ohshiro, K. Mitsui, N. Ando, Y. Ohsawa, W. Koinuma, H. Takahashi, S. Kondo, T. Nabeshima, and Y. Yano
Oxidation-active flavin models: Oxidation of α-hydroxy acids by benzo-dipteridine bearing metal-binding site in the presence of divalent metal ion and base in organic solvents
J. Am. Chem. Soc., 123, 2478-2486 (2001).
[134:337527]https://doi.org/10.1021/ja0009121 
 

S. Kondo, K. Shinbo, T. Yamaguchi, K. Yoshida, and Y. Yano
Cooperativity of binuclear Zn(II) complexes of imidazolyl ligands in the hydrolysis of bis(2,4-dinitrophenyl) phosphate in aqueous solution
J. Chem. Soc., Perkin Trans. 2, 128-131 (2001).
[134:266373]
 

H. Moriya, T. Kajiki, S. Watanabe, S. Kondo, and Y. Yano
Flavin receptors. Effect of the acidity of melamine derivatives bearing a 2-arylguanidinium ion on 6-azaflavin binding in chloroform
Bull. Chem. Soc. Jpn., 73, 2539-2542 (2000).
[134:100844]https://doi.org/10.1246/bcsj.73.2539
 

T. Hayashi, A. Fujimoto, T. Kajiki, S. Kondo, and Y. Yano
Functionalized flavin receptors. Bis-melamine derivatives bearing a guanidinium ion which bind 6-azaflavin and a thymnine-linked substrate through hydrogen bonds in chloroform
Chem. Lett., 1018 (2000).
[134:14466]
 

T. Kajiki, H. Moriya, K. Hoshino, T. Kuroi, S. Kondo, T. Nabeshima, and Y. Yano
Functionalized flavin receptors. Regulation of redox properties of 6-azaflavin via hydrogen bondings with melamine derivatives bearing guanidinium ion(s) in organic solvents
J. Org. Chem., 64, 9679-9689 (1999).
[132:107675]
 

H. Ohshiro, H. Takahashi, S. Kondo, Y. Yano, M. Koga, and F. Yoneda
Oxidation activity of long conjugative and metal-coordinative flavin model: Bent-benzodipteridine
Heterocycles, 51, 969-973 (1999).
 

T. Kajiki, H. Moriya, K. Hoshino, S. Kondo, Y. Yano
Regulation of redox properties of 6-azaflavin by hydrogen bonding with a receptor in chloroform-acetonitrile
Chem. Lett., 397-398 (1999).
 

S. Kondo, K. Yoshida, Y. Yano
Remarkable rate-accelerating metal-ion effect on intramolecular transesterification of phosphodiester in acetonitrile
J. Chem. Res. (S), 106 (1999).
https://doi.org/10.1039/a803986k 
 

Y. Kawai, K. Hida, M. Tsujimoto, S. Kondo, K. Kitano, K. Nakamura and A. Ohno
Asymmetric reduction of α-keto esters and α-diketones with a bakers' yeast keto ester reductase
Bull. Chem. Soc. Jpn., 72, 99-102 (1999).
https://doi.org/10.1246/bcsj.72.99 
 

T. Kajiki, H. Moriya, S. Kondo, T. Nabeshima and Y. Yano
Remarkable stabilization of the anionic semiquinone radical of 6-azaflavin by hydrogen bonding with a receptor in chloroform
Chem. Commun., 2727-2728 (1998).
 

H. Tamiaki, M. Kouraba, K. Takeda, S. Kondo and R. Tanikaga
Asymmetric synthesis of methyl bacteriopheophorbide-d and the analogs by stereoselective reduction of 3-acetyl to chiral 3-(1-hydroxyethyl) group
Tetrahedron: Asymmetry, 9, 2101-2111 (1998).
 

H. Ohshiro, N. Tamura, A. Arai, K. Yamaguchi, M. Taknobu, T. Tominami, S. Kondo, T. Nabeshima, Y. Yano, J. Toyoda, K. Nakasuji, P. F. Heelis
A novel property of reduced benzodipteridine toward molecular oxygen
Heterocycles, 48, 627 - 630 (1998).
 

K. Utsumi, Y. Nishihara, K. Hoshino, S. Kondo, T. Nabeshima, and Y. Yano
Bifunctional receptor. Rate-acceleration of oxidative decarboxylation of pyruvate by thymine-thiazolium and Zn2+ in the presence of a melamine derivative bearing α-bipyridine moiety in chloroform-acetonitrile
Chem. Lett., 1081 (1997).
 

S. Kondo, K. Utsumi, and Y. Yano
A novel probe for determination of association constants between barbituric acid derivatives and their receptors
Int. J. Chem. Chem. Biol., 1 (1997).
 

K. Nakamura, S. Kondo, Y. Kawai, N. Nakajima, and A. Ohno
Amino acid sequence and characterization of aldo-keto reductase from bakers' yeast
Biosci. Biotech. Biochem., 61, 375-377 (1997).
 

K. Ishihara, S. Kondo, K. Nakamura and Nobuyoshi Nakajima
Protein sequences of two keto ester reductases: Possible identity as hypothetical proteins
Biosci. Biotech. Biochem., 60, 1538-1539 (1996).
 

K. Nakamura, S. Kondo, Y. Kawai, K. Kitano, K. Hida, and A. Ohno
Enantio- and regioselective reduction of α-Diketones by baker's yeast
Tetrahedron: Asymmetry, 7, 409-412 (1996).
 

K. Nakamura, S. Kondo, Y. Kawai, N. Nakajima, and A. Ohno
Purification and characterization of α-keto ester reductases from bakers' yeast
Biosci. Biotech. Biochem., 58, 2236-2240 (1994).
 

K. Nakamura, S. Kondo, N. Nakajima, and A. Ohno
Mechanistic study for stereochemical control of microbial reduction of α-keto esters in an organic solvent
Tetrahedron, 51, 687-694 (1995).
https://doi.org/10.1016/0040-4020(94)00970-6
 

N. Nakajima, K. Ishihara, S. Tsuboi, M. Utaka, S. Kondo, and K. Nakamura
Two l stereoselective carbonyl reductases from bakers' yeast: Differences in protein structure and similarities in catalytic function
Biosci. Biotech. Biochem., 58, 2080-2081 (1994).
 

Y. Kawai, S. Kondo, M. Tsujimoto, K. Nakamura, and A. Ohno
Stereochemical control in microbial reduction. XXIII. Thermal treatment of bakers' yeast for controlling the stereoselectivity of reductions
Bull. Chem. Soc. Jpn., 67, 2244-2249 (1994).
https://doi.org/10.1246/bcsj.67.2244 
 

Y. Kawai, M. Tsujimoto, S. Kondo, K. Takanobe, K. Nakamura, and A. Ohno
Asymmetric Reduction of β-keto esters with an enzyme from bakers' yeast
Bull. Chem. Soc. Jpn., 67, 524-528 (1994).
https://doi.org/10.1246/bcsj.67.524
 

K. Nakamura, S. Kondo, A. Ohno
Effect of cyclodextrin on improvement of enantioselectivity in the reduction of ketopantolactone with bakers' yeast
Bioorg. Med. Chem., 2, 433-437 (1994).
 

K. Nakamura, S. Kondo, Y. Kawai, and A. Ohno
Stereochemical control in microbial reduction. XXI. Effect of organic solvent on reduction of α-keto esters mediated by bakers' yeast
Bull. Chem. Soc. Jpn., 66, 2738-2743 (1993).
https://doi.org/10.1246/bcsj.66.2738
 

K. Nakamura, S. Kondo, Y. Kawai, and A. Ohno
Asymmetric reduction of ketopantolactone by bakers' yeast
Tetrahedron: Asymmetry, 4,1253-1254 (1993).
 

K. Nakamura, S. Kondo, Y. Kawai, and A. Ohno
Reduction by bakers' yeast in benzene
Tetrahedron Lett., 32, 7075-7078 (1991).
https://doi.org/10.1016/0040-4039(91)85044-6