Page 64 - 《精细化工》2020年 第10期
P. 64
·1994· 精细化工 FINE CHEMICALS 第 37 卷
(thiophen-2-yl)naphtho[2,3-c][1,2,5]thiadiazole as new acceptor units [27] REID M, ROWEB D, TAYLOR R J. Two carbon homologated alpha,
for D-A type co-polymer for polymer solar cells[J]. Synthetic Metals, beta-unsaturated aldehydes from alcohols using the in situ oxidation-
2019, 252: 113-121. Wittig reaction[J]. Chemical Communications, 2003, 18: 2284-2285.
[8] ROCHA D H A, PINTO D C G A, SILVA A M S. Applications of the [28] MITSUNORI O, TOMOMI N, MIYAKO N, et al. A short-step
Wittig reaction on the synthesis of natural and natural-analogue synthesis of 1,6-methano[10]annulene-3,4-dicarboximides and their
heterocyclic compounds[J]. European Journal of Organic Chemistry, benzene-, naphthalene-, and thiophene-annulated compounds[J].
2018, 2018(20/21): 2443-2457. European Journal of Organic Chemistry. 2014, 27: 5976-5985.
[9] WU J L, WU H F, WEI A Y, et al. Highly regioselective Wittig [29] MÄRKL G, EHRL R, KREITMEIER P, et al. Superheteroaromaten
reactions of cyclic ketones with a stabilized phosphorus ylide under mit furan-bausteinen: Isomere antiaromatische tetraepoxy[36]annulene
controlled microwave heating[J]. Tetrahedron Letters, 2004, 45(22): (6.4.6.4) und aromatische tetraoxa[34] porphyrin(6.4.6.4)-dikationen
4401-4404. [J]. Helvetica Chimica Acta, 2000, 83(2): 495-511.
[10] KISS L, FORRO E, ORSY G, et al. Stereo- and regiocontrolled [30] JAN B, JAN S, CHRISTIAN N, et al. Synthesis of annulenes via
syntheses of exomethylenic cyclohexane β-amino acid derivatives[J]. multiple Wittig reactions: In-situ dimerization of 1,2;5,6-
Molecules, 2015, 20(12): 21094-21102. dibenzocyclooctatetraene[J]. European Journal of Organic Chemistry,
[11] VUONG W, MOSQUERA G F, SANICHAR R, et al. Synthesis of 2008, 9: 1619-1624.
chiral spin-labeled amino acids[J]. Organic Letters, 2019, 21(24): [31] ALAIME T, DANIEL M, HIEBEL M A, et al. Access to 1H-indazoles,
10149-10153. 1H-benzoindazoles and 1H-azaindazoles from (het) aryl azides: A
[12] SUGANUMA Y, SAITO S, KOBAYASHI Y. Synthesis of 8-HEPE staudinger-aza-Wittig tandem reaction leading to N— N bond
and 10-HDoHE in both (R)- and (S)-forms via Wittig reactions with formation[J]. Royal Society of chemistry, 2018, 54(60): 8411-8414.
COOH-Ylides[J]. Synlett, 2019, 30(3): 338-342. [32] YAN Y M, LI H Y, REN J, et al. One-pot selective synthesis of
[13] PRIMDAHL K G, AURSNES M, WALKER M E, et al. Synthesis of multisubstituted quinoxalin-2(1H)-ones by a Ugi 4CR/catalytic aza-
13(R)-hydroxy-7Z,10Z,13R,14E,16Z,19Z docosapentaenoic acid (13R- Wittig sequence[J]. Synlett, 2018, 29(11): 1447-1450.
HDPA) and its biosynthetic conversion to the 13-series resolvins[J]. [33] DANIELA K, HANA K, KAREL D, et al. Microwave-assisted
Journal of Natural Products, 2016, 79(10): 2693-2702. synthesis of phenylpropanoids and coumarins: Total synthesis of
[14] SANCEAU J, MALTAIS R, POIRIER D, et al. Total synthesis of the osthol[J]. European Journal of Organic Chemistry, 2017, (35): 5204-
antidiabetic (type 2) lipid mediator protectin DX/PDX[J]. The Journal 5213.
of Organic Chemistry, 2018, 84(2): 495-505. [34] NIGARADDI S B, NARAHARI D, MANJUNATH G S, et al. A
[15] XIA X S, LAO Z Q, TOY P. Triphenylphosphine oxide-catalyzed practical one-pot synthesis of coumarins in aqueous sodium bicarbonate
selective, α,β-reduction of conjugated polyunsaturated ketones[J]. via intramolecular Wittig reaction at room temperature[J]. Royal
Synlett, 2019, 30(9): 1100-1104. Society of Chemistry Advances, 2014, 4(75): 39667.
[16] YUMIKO Y, YUYA N, ATSUSHI A, et al. Total synthesis of [35] ALEXANDER J N, SERGIO R V, DENIS J C, et al. Synthesis of
lycopene-5,6-diol and γ-carotene-5',6'-diol stereoisomers and their α-methylstilbenes using an aqueous Wittig methodology and
HPLC separation[J]. Tetrahedron, 2017, 73(15): 2043-2052. application toward the development of potent human aromatase
[17] DING M W (丁明武), LIU Z J (刘钊杰). Recent advances in aza- inhibitors[J]. Bioorganic & Medicinal Chemistry Letters, 2019, 29(11):
Wittig reaction[J]. Chinese Journal of Organic Chemistry (有机化 1395-1398.
学), 2001, 21(1): 1-7. [36] RAPHAEL M F, DARIO N, JORG S. DNA-encoded chemical libraries:
[18] XIONG J, WEI X, LIU Z M, et al. One-pot synthesis of Advancing beyond conventional small-molecule libraries[J]. Accounts
polysubstituted imidazoles via sequential staudinger/aza-Wittig/Ag(Ⅰ) of Chemical Research, 2014, 47(4): 1247-1255.
catalyzed cyclization/isomerization[J]. The Journal of Organic [37] BATHULA R, CHANDAN K, PREMKUMAR G, et al. Computational
Chemistry, 2017, 82(24): 13735-13739. studies on G-quadruplex DNA-stabilizing property of novel Wittig-
[19] GUAN Z R, LIU Z M, DING M W. New efficient synthesis of 1H- based Schiff-base ligands and their copper (Ⅱ) complexes[J]. Structural
imidazo-[4,5-c] quinolines by a sequential Van Leusen/Staudinger/ Chemistry, 2019, 30(3): 727-742.
aza-Wittig/carbodiimide mediated cyclization[J]. Tetrahedron, 2018, [38] VERENA B K K, CHRITIANE E, ALEXANDER D, et al.
74(50): 7186-7192. Isocyanide multicomponent reactions on solid-phase-coupled DNA
[20] GUAN Z R, LIU S, LIU Z M, et al. One-pot three-component oligonucleotides for encoded library synthesis[J]. Organic Letters,
synthesis of pyrrolidin-2-ones via a sequential Wittig/nucleophilic 2019, 21(18): 7238-7243.
addition/cyclization reaction[J]. Synthesis, 2019, 51(11): 2402-2408. [39] VIVIAN T, RATMIR D. Tandem Wittig/Diels-Alder diversification
[21] HUANG B, HU D Q, WANG J, et al. Copper-catalyzed one-pot of genetically encoded peptide libraries[J]. Organic & Biomolecular
tandem reactions toward the synthesis of indoles using o-iodoanilines, Chemistry, 2017, 15(37): 7869-7877.
acyl chlorides and Wittig reagents[J]. Tetrahedron Letters, 2015, 56(20): [40] ZHOU Q, LI K, LI L L, et al. Combining Wittig olefination with
2551-2554. photoassisted domino reaction to distinguish 5-formylcytosine from
[22] JACOBT H, WAH C B, JASIM M A A. Synthesis of (E)-10- 5-formyluracil[J]. Analytical Chemistry, 2019, 91(15): 9366-9370.
hydroxy-2-decenoic acid ethyl ester via a one-pot tandem oxidation- [41] KENJI M. Pheromone synthesis. Part 257: Synthesis of methyl
Wittig process[J]. Organic Communications, 2018, 11(3): 168-172. (2E,4Z,7Z)-2,4,7-decatrienoate and methyl (E)-2,4,5-tetradecatrienoate,
[23] DENG C, ZHOU J L, LIU H K, et al. Rh 2(OAc) 4 catalyzed Wittig- the pheromone components of the male dried bean beetle,
type olefination: A facile access to alkylidene and arylidene malonates[J]. Acanthoscelides obtectus (Say)[J]. Tetrahedron, 2015, 71(34): 5589-
Chinese Journal of Organic Chemistry, 2019, 39(8): 2328-2332. 5596.
[24] MARIE L S, SVEN A, THOMAS W. First base-free catalytic Wittig [42] YANG X M (杨晓梅), ZHANG Y S (张玉顺), YAO B (姚赟), et al.
reaction[J]. Organic Letters, 2015, 17(12): 3078-3081. Simple synthesis of (Z)-7-eicosen-11-one—the sex pheromone of
[25] SCHIRMER M, ADOMEIT S, SPANNENBERG A, et al. Novel base- peach fruit moth[J]. Chinese Journal of Organic Chemistry (有机化
free catalytic Wittig reaction for the synthesis of highly functionalized 学), 2014, 34: 1458-1461.
alkenes[J]. Chemistry-A European Journal, 2016, 22(7): 2458-2465. [43] JUNHEON K, DONG S K, SHIGERU M, et al. Development of a
[26] LONGWITZ L, SPANNENBERG A, WERNER T. Phosphetane oxides pheromone trap for monitor black pine bast scale, Matsucoccus
as redox cycling catalysts in the catalytic Wittig reaction at room thunbergianae (Hemiptera: Margarodidae)[J]. Journal of Asia-Pacific
temperature[J]. Journal of the American Chemical Society Catalysis, Entomology, 2016, 19(3): 899-902.
2019, 9(10): 9237-9244. (下转第 2040 页)