Topics in Current Chemistry (2019) 377:1
1 3
74. Upare PP, Yoon JW, Hwang DW et al (2016) Design of a heterogeneous catalytic process for the
continuous and direct synthesis of lactide from lactic acid. Green Chem 18:5978–5983
75. De Clercq R, Dusselier M, Makshina E, Sels BF (2018) Catalytic gas‑phase production of lactide
from renewable alkyl lactates. Angew Chem Int Ed 57:3074–3078
76. De Clercq R, Dusselier M, Poleunis C, Debecker DP, Giebeler L, Oswald S, Makshina E, Sels BF
(2018) Titania–silica catalysts for lactide production from renewable alkyl lactates: structure–activ‑
ity relations. ACS Catal 8:8130–8139
77. Banerjee A, Dick GR, Yoshino T, Kanan MW (2016) Carbon dioxide utilization via carbonate‑
promoted C–H carboxylation. Nature 531:215–219
78. Lilga MA, Hallen RT, Gray M (2010) Production of oxidized derivatives of 5‑hydroxymethylfur‑
fural (HMF). Top Catal 53:1264–1269
79. Arntz D, Fischer A, Höpp M, Jacobi S, Sauer J, Ohara T, Sato T, Shimizu N, Schwind H (2007)
Acrolein and methacrolein. In: Ullmann’s Editorial Advisory Board (eds) Ullmann’s encyclopedia
of industrial chemistry. Wiley‑VCH, Weinheim, pp 329–346
80. Katryniok B, Paul S, Dumeignil F (2013) Recent developments in the field of catalytic dehydration
of glycerol to acrolein. ACS Catal 3:1819–1834
81. Deleplanque J, Dubois J‑L, Devaux J‑F, Ueda W (2010) Production of acrolein and acrylic acid
through dehydration and oxydehydration of glycerol with mixed oxide catalysts. Catal Today
157:351–358
82. Yun D, Kim TY, Park DS, Yun YS, Han JW, Yi J (2014) A tailored catalyst for the sustainable
conversion of glycerol to acrolein: mechanistic aspect of sequential dehydration. ChemSusChem
7:2193–2201
83. Ma T, Yun Z, Xu W, Chen L, Li L, Ding J, Shao R (2016) Pd‑H3PW12O40/Zr‑MCM‑41: an effi‑
cient catalyst for the sustainable dehydration of glycerol to acrolein. Chem Eng J 294:343–352
84. Huang L, Qin F, Huang Z, Zhuang Y, Ma J, Xu H, Shen W (2016) Hierarchical ZSM‑5 zeolite
synthesized by an ultrasound‑assisted method as a long‑life catalyst for dehydration of glycerol to
acrolein. Ind Eng Chem Res 55:7318–7327
85. Krähling L, Krey J, Jakobson G, Grolig J, Miksche L (2000) Allyl compounds. In: Ullmann’s Edi‑
torial Advisory Board (eds) Ullmann’s encyclopedia of industrial chemistry. Wiley‑VCH, Wein‑
heim, pp 447–469
86. Tshibalonza NN, Monbaliu J‑CM (2017) Revisiting the deoxydehydration of glycerol towards allyl
alcohol under continuous‑flow conditions. Green Chem 19:3006–3013
87. Heugebaert TSA, Stevens CV, Kappe CO (2015) Singlet‑oxygen oxidation of 5‑hydroxymethylfur‑
fural in continuous flow. ChemSusChem 8:1648–1651
88. Aellig C, Scholz D, Conrad S, Hermans I (2013) Intensification of TEMPO‑mediated aerobic alco‑
hol oxidations under three‑phase flow conditions. Green Chem 15:1975–1980
89. Liu K, Huang X, Pidko EA, Hensen EJM (2017) MoO 3 –TiO 2 synergy in oxidative dehydrogena‑
tion of lactic acid to pyruvic acid. Green Chem 19:3014–3022
90. Allais C, Grassot J‑M, Rodriguez J, Constantieux T (2014) Metal‑free multicomponent syntheses
of pyridines. Chem Rev 114:10829–10868
91. Luo CW, Huang C, Li A, Yi W‑J, Feng X‑Y, Xu Z‑J, Chao Z‑S (2016) Influence of reaction param‑
eters on the catalytic performance of alkaline‑treated zeolites in the novel synthesis of pyridine
bases from glycerol and ammonia. Ind Eng Chem Res 55:893–911
92. Li A, Huang C, Luo C‑W, Yi W‑J, Chao Z‑S (2017) High‑efficiency catalytic performance over
mesoporous Ni/beta zeolite for the synthesis of quinoline from glycerol and aniline. RSC Adv
7:9551–9561
93. Gribble GW (ed) (2010) Heterocyclic scaffolds II: reactions and application of indoles. Springer,
Berlin
94. Yao Q, Xu L, Zhang Y, Fu Y (2016) Enhancement of indoles production and catalyst stability in
thermo‑catalytic conversion and ammonization of furfural with NH 3 and N 2 environments. J Anal
Appl Pyrolysis 121:258–266
95. Venugopal A, Sarkari R, Anjaneyulu C, Krishna V, Kumar MK, Narender N, Padmasri AH (2014)
Influence of acid‑base sites on ZnO–ZnCr 2 O 4 catalyst during dehydrocyclization of aqueous glyc‑
erol and ethylenediamine for the synthesis of 2‑methylpyrazine: kinetic and mechanism studies.
Appl Catal A Gen 469:398–409
96. Hoydonckx HE, Van Rhijn WM, Van Rhijn W, De Vos DE, Jacobs PA (2007) Furfural and deriva‑
tives. In: Ullmann’s Editorial Advisory Board (eds) Ullmann’s encyclopedia of industrial chemis‑
try. Wiley‑VCH, Weinheim, pp 285–313
144
Reprinted from the journal
1 3
74. Upare PP, Yoon JW, Hwang DW et al (2016) Design of a heterogeneous catalytic process for the
continuous and direct synthesis of lactide from lactic acid. Green Chem 18:5978–5983
75. De Clercq R, Dusselier M, Makshina E, Sels BF (2018) Catalytic gas‑phase production of lactide
from renewable alkyl lactates. Angew Chem Int Ed 57:3074–3078
76. De Clercq R, Dusselier M, Poleunis C, Debecker DP, Giebeler L, Oswald S, Makshina E, Sels BF
(2018) Titania–silica catalysts for lactide production from renewable alkyl lactates: structure–activ‑
ity relations. ACS Catal 8:8130–8139
77. Banerjee A, Dick GR, Yoshino T, Kanan MW (2016) Carbon dioxide utilization via carbonate‑
promoted C–H carboxylation. Nature 531:215–219
78. Lilga MA, Hallen RT, Gray M (2010) Production of oxidized derivatives of 5‑hydroxymethylfur‑
fural (HMF). Top Catal 53:1264–1269
79. Arntz D, Fischer A, Höpp M, Jacobi S, Sauer J, Ohara T, Sato T, Shimizu N, Schwind H (2007)
Acrolein and methacrolein. In: Ullmann’s Editorial Advisory Board (eds) Ullmann’s encyclopedia
of industrial chemistry. Wiley‑VCH, Weinheim, pp 329–346
80. Katryniok B, Paul S, Dumeignil F (2013) Recent developments in the field of catalytic dehydration
of glycerol to acrolein. ACS Catal 3:1819–1834
81. Deleplanque J, Dubois J‑L, Devaux J‑F, Ueda W (2010) Production of acrolein and acrylic acid
through dehydration and oxydehydration of glycerol with mixed oxide catalysts. Catal Today
157:351–358
82. Yun D, Kim TY, Park DS, Yun YS, Han JW, Yi J (2014) A tailored catalyst for the sustainable
conversion of glycerol to acrolein: mechanistic aspect of sequential dehydration. ChemSusChem
7:2193–2201
83. Ma T, Yun Z, Xu W, Chen L, Li L, Ding J, Shao R (2016) Pd‑H3PW12O40/Zr‑MCM‑41: an effi‑
cient catalyst for the sustainable dehydration of glycerol to acrolein. Chem Eng J 294:343–352
84. Huang L, Qin F, Huang Z, Zhuang Y, Ma J, Xu H, Shen W (2016) Hierarchical ZSM‑5 zeolite
synthesized by an ultrasound‑assisted method as a long‑life catalyst for dehydration of glycerol to
acrolein. Ind Eng Chem Res 55:7318–7327
85. Krähling L, Krey J, Jakobson G, Grolig J, Miksche L (2000) Allyl compounds. In: Ullmann’s Edi‑
torial Advisory Board (eds) Ullmann’s encyclopedia of industrial chemistry. Wiley‑VCH, Wein‑
heim, pp 447–469
86. Tshibalonza NN, Monbaliu J‑CM (2017) Revisiting the deoxydehydration of glycerol towards allyl
alcohol under continuous‑flow conditions. Green Chem 19:3006–3013
87. Heugebaert TSA, Stevens CV, Kappe CO (2015) Singlet‑oxygen oxidation of 5‑hydroxymethylfur‑
fural in continuous flow. ChemSusChem 8:1648–1651
88. Aellig C, Scholz D, Conrad S, Hermans I (2013) Intensification of TEMPO‑mediated aerobic alco‑
hol oxidations under three‑phase flow conditions. Green Chem 15:1975–1980
89. Liu K, Huang X, Pidko EA, Hensen EJM (2017) MoO 3 –TiO 2 synergy in oxidative dehydrogena‑
tion of lactic acid to pyruvic acid. Green Chem 19:3014–3022
90. Allais C, Grassot J‑M, Rodriguez J, Constantieux T (2014) Metal‑free multicomponent syntheses
of pyridines. Chem Rev 114:10829–10868
91. Luo CW, Huang C, Li A, Yi W‑J, Feng X‑Y, Xu Z‑J, Chao Z‑S (2016) Influence of reaction param‑
eters on the catalytic performance of alkaline‑treated zeolites in the novel synthesis of pyridine
bases from glycerol and ammonia. Ind Eng Chem Res 55:893–911
92. Li A, Huang C, Luo C‑W, Yi W‑J, Chao Z‑S (2017) High‑efficiency catalytic performance over
mesoporous Ni/beta zeolite for the synthesis of quinoline from glycerol and aniline. RSC Adv
7:9551–9561
93. Gribble GW (ed) (2010) Heterocyclic scaffolds II: reactions and application of indoles. Springer,
Berlin
94. Yao Q, Xu L, Zhang Y, Fu Y (2016) Enhancement of indoles production and catalyst stability in
thermo‑catalytic conversion and ammonization of furfural with NH 3 and N 2 environments. J Anal
Appl Pyrolysis 121:258–266
95. Venugopal A, Sarkari R, Anjaneyulu C, Krishna V, Kumar MK, Narender N, Padmasri AH (2014)
Influence of acid‑base sites on ZnO–ZnCr 2 O 4 catalyst during dehydrocyclization of aqueous glyc‑
erol and ethylenediamine for the synthesis of 2‑methylpyrazine: kinetic and mechanism studies.
Appl Catal A Gen 469:398–409
96. Hoydonckx HE, Van Rhijn WM, Van Rhijn W, De Vos DE, Jacobs PA (2007) Furfural and deriva‑
tives. In: Ullmann’s Editorial Advisory Board (eds) Ullmann’s encyclopedia of industrial chemis‑
try. Wiley‑VCH, Weinheim, pp 285–313
144
Reprinted from the journal