Relevant bibliographies by topics / Dieno de Brassard / Journal articles
To see the other types of publications on this topic, follow the link: Dieno de Brassard.

Journal articles on the topic 'Dieno de Brassard'

Author: Grafiati
Published: 9 September 2021
Last updated: 29 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 31 journal articles for your research on the topic 'Dieno de Brassard.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Fan, Qian, Lili Lin, Jie Liu, Yaozong Huang, Xiaoming Feng, and Guolin Zhang. "Highly Enantioselective Hetero-Diels−Alder Reaction of Brassard Diene with Aromatic Aldehydes." Organic Letters 6, no. 13 (2004): 2185–88. http://dx.doi.org/10.1021/ol049364c.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Lin, Lili, Yulong Kuang, Xiaohua Liu, and Xiaoming Feng. "Indium(III)-Catalyzed Asymmetric Hetero-Diels–Alder Reaction of Brassard-Type Diene with Aliphatic Aldehydes." Organic Letters 13, no. 15 (2011): 3868–71. http://dx.doi.org/10.1021/ol2013999.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Fan, Qian, Lili Lin, Jie Liu, Yaozong Huang, and Xiaoming Feng. "A Mild and Efficient Asymmetric Hetero-Diels-Alder Reaction of the Brassard Diene with Aldehydes." European Journal of Organic Chemistry 2005, no. 16 (2005): 3542–52. http://dx.doi.org/10.1002/ejoc.200500126.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Akiyama, T., J. Itoh, and K. Fuchibe. "Enantioselective Aza-Diels-Alder Reaction of Brassard’s Diene with Imines." Synfacts 2006, no. 9 (2006): 0948. http://dx.doi.org/10.1055/s-2006-949224.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

WALDMANN, H., M. BRAUN, and M. DRAEGER. "ChemInform Abstract: Asymmetric Aza Diels-Alder Reactions of Amino Acid Ester Imines with Brassard′s Diene." ChemInform 23, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199214077.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Lin, Lili, Yulong Kuang, Xiaohua Liu, and Xiaoming Feng. "ChemInform Abstract: Indium(III)-Catalyzed Asymmetric Hetero-Diels-Alder Reaction of Brassard-Type Diene with Aliphatic Aldehydes." ChemInform 42, no. 49 (2011): no. http://dx.doi.org/10.1002/chin.201149129.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Mukaiyama, Teruaki, Yuji Maruyama, and Takayuki Kitazawa. "A New Synthesis of Dihydropyridin-2-ones from Brassard’s Diene and Imines." HETEROCYCLES 76, no. 1 (2008): 221. http://dx.doi.org/10.3987/com-08-s(n)51.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

LOCK, R., and H. WALDMANN. "ChemInform Abstract: Construction of Tetracyclic Indole Bases via Aza Diels-Alder Reaction of Indolylethylimines with Brassard′s Diene." ChemInform 25, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199440225.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Waldmann, Herbert, Matthias Braun, and Martin Dräger. "Asymmetric aza Diels-Alder reactions of amino acid ester imines with Brassard's diene." Tetrahedron: Asymmetry 2, no. 12 (1991): 1231–46. http://dx.doi.org/10.1016/s0957-4166(00)80023-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Zheng, Jianfeng, Lili Lin, Kai Fu, Haifeng Zheng, Xiaohua Liu, and Xiaoming Feng. "Synthesis of Optically Pure Spiro[cyclohexane-oxindoline] Derivatives via Catalytic Asymmetric Diels–Alder Reaction of Brassard-Type Diene with Methyleneindolines." Journal of Organic Chemistry 80, no. 17 (2015): 8836–42. http://dx.doi.org/10.1021/acs.joc.5b01318.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

Itoh, Junji, Kohei Fuchibe, and Takahiko Akiyama. "Chiral Brønsted Acid Catalyzed Enantioselective Aza-Diels–Alder Reaction of Brassard's Diene with Imines." Angewandte Chemie 118, no. 29 (2006): 4914–16. http://dx.doi.org/10.1002/ange.200601345.

Full text
APA, Harvard, Vancouver, ISO, and other styles
12

Itoh, Junji, Kohei Fuchibe, and Takahiko Akiyama. "Chiral Brønsted Acid Catalyzed Enantioselective Aza-Diels–Alder Reaction of Brassard's Diene with Imines." Angewandte Chemie International Edition 45, no. 29 (2006): 4796–98. http://dx.doi.org/10.1002/anie.200601345.

Full text
APA, Harvard, Vancouver, ISO, and other styles
13

Moriyama, Mizuki, Kohei Nakata, Tetsuya Fujiwara, and Yoo Tanabe. "Divergent Asymmetric Total Synthesis of All Four Pestalotin Diastereomers from (R)-Glycidol." Molecules 25, no. 2 (2020): 394. http://dx.doi.org/10.3390/molecules25020394.

Full text
Abstract:
All four chiral pestalotin diastereomers were synthesized in a straightforward and divergent manner from common (R)-glycidol. Catalytic asymmetric Mukaiyama aldol reactions of readily-available bis(TMSO)diene (Chan’s diene) with (S)-2-benzyloxyhexanal derived from (R)-glycidol produced a syn-aldol adduct with high diastereoselectivity and enantioselectivity using a Ti(iOPr)4/(S)-BINOL/LiCl catalyst. Diastereoselective Mukaiyama aldol reactions mediated by catalytic achiral Lewis acids directly produced not only a (1′S,6S)-pyrone precursor via the syn-aldol adduct using TiCl4, but also (1′S,6R)
APA, Harvard, Vancouver, ISO, and other styles
14

Wang, Guowei, Jinfeng Zhao, Yuhan Zhou, Baomin Wang, and Jingping Qu. "ChemInform Abstract: Mild and Highly Enantioselective Vinylogous Aldol Reaction of Brassard′s Diene with Aromatic Aldehydes by Combined Lewis Acid Catalyst." ChemInform 41, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.201049062.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

Lock, Ralf, and Herbert Waldmann. "Construction of tetracyclic indole bases via Aza Diels-Alder reaction of indolylethylimines with Brassard's diene." Liebigs Annalen der Chemie 1994, no. 5 (1994): 511–16. http://dx.doi.org/10.1002/jlac.15619940511.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

Zheng, Jianfeng, Lili Lin, Kai Fu, Haifeng Zheng, Xiaohua Liu, and Xiaoming Feng. "ChemInform Abstract: Synthesis of Optically Pure Spiro[cyclohexane-oxindoline] Derivatives via Catalytic Asymmetric Diels-Alder Reaction of Brassard-Type Diene with Methyleneindolines." ChemInform 47, no. 5 (2016): no. http://dx.doi.org/10.1002/chin.201605127.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Gu, Chun-Ling, Li Liu, Dong Wang та Yong-Jun Chen. "Facile Synthesis of δ-Amino-β-ketoesters and Piperidinediones via a Vinylogous Mannich-Type Reaction of Brassard-Type Diene with Aldimines without Catalyst". Synthetic Communications 39, № 16 (2009): 2989–3002. http://dx.doi.org/10.1080/00397910902730846.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

Chen, Zhenling, Lili Lin, Donghui Chen, Jiangting Li, Xiaohua Liu, and Xiaoming Feng. "ChemInform Abstract: Enantioselective Aza-Diels-Alder Reaction of Brassard′s Diene with Aldimines Catalyzed by Chiral N,N′-Dioxide-Yb(OTf)3 Complex." ChemInform 41, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.201039141.

Full text
APA, Harvard, Vancouver, ISO, and other styles
19

Wang, Guowei, Jinfeng Zhao, Yuhan Zhou, Baomin Wang, and Jingping Qu. "Mild and Highly Enantioselective Vinylogous Aldol Reaction of Brassard’s Diene with Aromatic Aldehydes by Combined Lewis Acid Catalyst." Journal of Organic Chemistry 75, no. 15 (2010): 5326–29. http://dx.doi.org/10.1021/jo100674f.

Full text
APA, Harvard, Vancouver, ISO, and other styles
20

Chen, Zhenling, Lili Lin, Donghui Chen, Jiangting Li, Xiaohua Liu, and Xiaoming Feng. "Enantioselective aza-Diels–Alder reaction of Brassard’s diene with aldimines catalyzed by chiral N,N′-dioxide–Yb(OTf)3 complex." Tetrahedron Letters 51, no. 23 (2010): 3088–91. http://dx.doi.org/10.1016/j.tetlet.2010.04.009.

Full text
APA, Harvard, Vancouver, ISO, and other styles
21

Lin, Lili, Zhenling Chen, Xu Yang, Xiaohua Liu, and Xiaoming Feng. "Efficient Enantioselective Hetero-Diels−Alder Reaction of Brassard's Diene with Aliphatic Aldehydes: A One-Step Synthesis of (R)-(+)-Kavain and (S)-(+)-Dihydrokavain." Organic Letters 10, no. 6 (2008): 1311–14. http://dx.doi.org/10.1021/ol8002282.

Full text
APA, Harvard, Vancouver, ISO, and other styles
22

Du, Haifeng, Dongbo Zhao, and Kuiling Ding. "Enantioselective Catalysis of the Hetero-Diels-Alder Reaction between Brassard's Diene and Aldehydes by Hydrogen-Bonding Activation: A One-Step Synthesis of (S)-(+)-Dihydrokawain." Chemistry - A European Journal 10, no. 23 (2004): 5964–70. http://dx.doi.org/10.1002/chem.200400515.

Full text
APA, Harvard, Vancouver, ISO, and other styles
23

Du, Haifeng, Dongbo Zhao, and Kuiling Ding. "Enantioselective Catalysis of the Hetero-Diels-Alder Reaction between Brassard's Diene and Aldehydes by Hydrogen-Bonding Activation: A One-Step Synthesis of (S)-(+)-Dihydrokawain." Chemistry - A European Journal 11, no. 7 (2005): 1975. http://dx.doi.org/10.1002/chem.200590022.

Full text
APA, Harvard, Vancouver, ISO, and other styles
24

Su, Zhishan, Song Qin, Changwei Hu, and Xiaoming Feng. "Theoretical Investigations on the Mechanism of Hetero-Diels-Alder Reactions of Brassard’s Diene and 1, 3-Butadiene Catalyzed by a Tridentate Schiff Base Titanium(IV) Complex." Chemistry - A European Journal 16, no. 14 (2010): 4359–67. http://dx.doi.org/10.1002/chem.200902488.

Full text
APA, Harvard, Vancouver, ISO, and other styles
25

Fan, Qian, Lili Lin, Jie Liu, Yaozong Huang, Xiaoming Feng, and Guolin Zhang. "Highly Enantioselective Hetero-Diels—Alder Reaction of Brassard Diene with Aromatic Aldehydes." ChemInform 35, no. 41 (2004). http://dx.doi.org/10.1002/chin.200441135.

Full text
APA, Harvard, Vancouver, ISO, and other styles
26

Fan, Qian, Lili Lin, Jie Liu, Yaozong Huang, and Xiaoming Feng. "A Mild and Efficient Asymmetric Hetero-Diels—Alder Reaction of the Brassard Diene with Aldehydes." ChemInform 36, no. 50 (2005). http://dx.doi.org/10.1002/chin.200550129.

Full text
APA, Harvard, Vancouver, ISO, and other styles
27

Itoh, Junji, Kohei Fuchibe, and Takahiko Akiyama. "Chiral Broensted Acid Catalyzed Enantioselective Aza-Diels—Alder Reaction of Brassard′s Diene with Imines." ChemInform 37, no. 46 (2006). http://dx.doi.org/10.1002/chin.200646179.

Full text
APA, Harvard, Vancouver, ISO, and other styles
28

Mukaiyama, Teruaki, Yuji Maruyama, and Takayuki Kitazawa. "ChemInform Abstract: A New Synthesis of Dihydropyridin-2-ones from Brassard′s Diene and Imines." ChemInform 40, no. 9 (2009). http://dx.doi.org/10.1002/chin.200909142.

Full text
APA, Harvard, Vancouver, ISO, and other styles
29

"Hetero-Diels-Alder Reaction of Brassard’s Diene and Aliphatic Aldehydes." Synfacts 2011, no. 11 (2011): 1212. http://dx.doi.org/10.1055/s-0031-1289180.

Full text
APA, Harvard, Vancouver, ISO, and other styles
30

Lin, Lili, Zhenling Chen, Xu Yang, Xiaohua Liu, and Xiaoming Feng. "ChemInform Abstract: Efficient Enantioselective Hetero-Diels-Alder Reaction of Brassard′s Diene with Aliphatic Aldehydes: A One-Step Synthesis of (R)-(+)-Kavain and (S)-(+)-Dihydrokavain." ChemInform 39, no. 36 (2008). http://dx.doi.org/10.1002/chin.200836134.

Full text
APA, Harvard, Vancouver, ISO, and other styles
31

Gu, Chun-Ling, Li Liu, Dong Wang, and Yong-Jun Chen. "ChemInform Abstract: Facile Synthesis of δ-Amino-β-ketoesters and Piperidinediones via a Vinylogous Mannich-Type Reaction of Brassard-Type Diene with Aldimines Without Catalyst." ChemInform 41, no. 5 (2010). http://dx.doi.org/10.1002/chin.201005127.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography