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1

Wood, E. "Stereochemistry." Biochemistry and Molecular Biology Education 29, no. 5 (September 2001): 216. http://dx.doi.org/10.1016/s1470-8175(01)00068-6.

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2

Mohd, Sharique Katchhi* Disha Kumareshi Harshitha M. V. Chakure Aditya Abrar Ahmed5. "The Role Of Stereochemistry And Formulation In Pharmacology Of The Drug." International Journal in Pharmaceutical Sciences 2, no. 3 (March 21, 2024): 790–802. https://doi.org/10.5281/zenodo.10850235.

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Abstract (sommario):
Stereochemistry profoundly influences the pharmacological properties of various drug classes, including antipsychotics, cardiovascular drugs, antibiotics, and antivirals. This review explores the impact of stereochemistry on drug efficacy, safety, and formulation across these therapeutic categories. Enantiomeric differences in drugs such as citalopram and beta-blockers highlight the significance of selecting the more active stereoisomer for improved clinical outcomes. Advanced drug formulations, including extended-release options and novel delivery systems, offer enhanced convenience and efficacy, particularly in antipsychotic and cardiovascular therapy. In the realm of anticancer drugs, understanding stereochemistry aids in the development of more potent and selective agents, while in antibiotics, it sheds light on mechanisms of action and resistance. Antiviral drug research emphasizes the importance of stereochemistry in optimizing drug design, metabolism, and formulation to combat infectious diseases effectively. Notably, advancements in nanotechnology offer promising avenues for improving antiviral therapies. This comprehensive exploration underscores the critical role of stereochemistry in drug development and optimization across diverse therapeutic areas, shaping the future of pharmacotherapy.
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3

Agami, Claude, and Toufic Rizk. "Stereochemistry-60." Tetrahedron 41, no. 3 (January 1985): 537–40. http://dx.doi.org/10.1016/s0040-4020(01)96496-8.

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4

Walba, David M. "Topological stereochemistry." Tetrahedron 41, no. 16 (January 1985): 3161–212. http://dx.doi.org/10.1016/s0040-4020(01)96671-2.

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5

Shallenberger, Robert S., and Wanda J. Wienen. "Carbohydrate stereochemistry." Journal of Chemical Education 66, no. 1 (January 1989): 67. http://dx.doi.org/10.1021/ed066p67.

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6

Gibb, Bruce C. "Supramolecular Stereochemistry." Journal of Supramolecular Chemistry 2, no. 1-3 (January 2002): 123–31. http://dx.doi.org/10.1016/s1472-7862(02)00088-6.

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7

Kellogg, Richard M. "Practical Stereochemistry." Accounts of Chemical Research 50, no. 4 (March 2017): 905–14. http://dx.doi.org/10.1021/acs.accounts.6b00630.

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8

"Stereochemistry." Carbohydrate Polymers 50, no. 1 (October 1, 2002): 96. http://dx.doi.org/10.1016/s0144-8617(01)00368-x.

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9

Kusumaningdyah, Rooserina, Iztok Devetak, Yudhi Utomo, Effendy Effendy, Daratu Putri, and Habiddin Habiddin. "Teaching Stereochemistry with Multimedia and Hands-On Models: The Relationship between Students’ Scientific Reasoning Skills and The Effectiveness of Model Type." Center for Educational Policy Studies Journal, May 31, 2023. http://dx.doi.org/10.26529/cepsj.1547.

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This paper presents an analysis of the use of multimedia and hands-on models on university students’ understanding of stereochemistry. The relationship between students’ scientific reasoning skills and their understanding of stereochemistry was also determined. Two groups of second-year chemistry students from the State University of Malang taking organic chemistry for the 2020/21 academic year participated in this study. One group of students experienced stereochemistry teaching using multimedia models and the other hands-on models as the learning medium. Lawson’s Classroom Test of Scientific Reasoning and Short-Answer Stereochemistry Test were applied. The former was deployed to measure students’ scientific reasoning skills, while the latter was used to test their understanding of stereochemistry. The results revealed that the students’ scientific reasoning skills were significantly below the expected standard, falling in the low category. Students with high scientific reasoning skills exhibited a better understanding of stereochemistry than those with low levels. Both multimedia and hands-on models revealed an equal contribution towards students’ understanding of stereochemistry. Also, it suggests that multimedia models tend to favour students with high scientific reasoning skills, while hands-on models favour those with low skills.
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10

Ippoliti, Francesca M., Melinda M. Nguyen, Amber J. Reilly, and Neil K. Garg. "Gaming stereochemistry." Nature Reviews Chemistry, May 12, 2022. http://dx.doi.org/10.1038/s41570-022-00395-5.

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11

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 3 (February 2003): A49—A72. http://dx.doi.org/10.1016/s0957-4166(03)00062-4.

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12

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 4 (February 2003): A73—A100. http://dx.doi.org/10.1016/s0957-4166(03)00110-1.

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13

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 5 (March 2003): A101—A129. http://dx.doi.org/10.1016/s0957-4166(03)00143-5.

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14

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 6 (March 2003): A131—A156. http://dx.doi.org/10.1016/s0957-4166(03)00189-7.

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15

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 7 (April 2003): A157—A181. http://dx.doi.org/10.1016/s0957-4166(03)00233-7.

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16

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 8 (April 2003): A183—A204. http://dx.doi.org/10.1016/s0957-4166(03)00266-0.

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17

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 9 (May 2003): A205—A239. http://dx.doi.org/10.1016/s0957-4166(03)00299-4.

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18

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 10 (May 2003): A241—A267. http://dx.doi.org/10.1016/s0957-4166(03)00340-9.

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19

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 11 (June 2003): A269—A301. http://dx.doi.org/10.1016/s0957-4166(03)00386-0.

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20

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 12 (June 2003): A303—A336. http://dx.doi.org/10.1016/s0957-4166(03)00422-1.

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21

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 13 (July 2003): A337—A372. http://dx.doi.org/10.1016/s0957-4166(03)00469-5.

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22

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 14 (July 2003): A373—A404. http://dx.doi.org/10.1016/s0957-4166(03)00512-3.

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23

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 15 (August 2003): A405—A437. http://dx.doi.org/10.1016/s0957-4166(03)00561-5.

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24

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 16 (August 2003): A439—A457. http://dx.doi.org/10.1016/s0957-4166(03)00611-6.

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25

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 17 (September 2003): A459—A498. http://dx.doi.org/10.1016/s0957-4166(03)00672-4.

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26

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 18 (September 2003): A499—A526. http://dx.doi.org/10.1016/s0957-4166(03)00705-5.

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27

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 19 (October 2003): A527—A557. http://dx.doi.org/10.1016/s0957-4166(03)00772-9.

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28

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 20 (October 2003): A559—A611. http://dx.doi.org/10.1016/s0957-4166(03)00816-4.

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29

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 21 (October 2003): A613—A644. http://dx.doi.org/10.1016/s0957-4166(03)00844-9.

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30

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 22 (November 2003): A645—A667. http://dx.doi.org/10.1016/s0957-4166(03)00878-4.

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31

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 23 (November 2003): A669—A707. http://dx.doi.org/10.1016/s0957-4166(03)00921-2.

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32

"Stereochemistry abstracts." Tetrahedron: Asymmetry 14, no. 24 (December 2003): A709—A747. http://dx.doi.org/10.1016/s0957-4166(03)00962-5.

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33

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 1 (January 2004): A1—A33. http://dx.doi.org/10.1016/s0957-4166(03)01009-7.

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34

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 2 (January 2004): A35—A73. http://dx.doi.org/10.1016/s0957-4166(04)00015-1.

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35

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 3 (February 2004): A75—A112. http://dx.doi.org/10.1016/s0957-4166(04)00061-8.

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36

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 4 (February 2004): A113—A146. http://dx.doi.org/10.1016/s0957-4166(04)00102-8.

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37

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 5 (March 2004): A147—A183. http://dx.doi.org/10.1016/s0957-4166(04)00133-8.

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38

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 6 (March 2004): A185—A211. http://dx.doi.org/10.1016/s0957-4166(04)00156-9.

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39

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 7 (April 2004): A213—A246. http://dx.doi.org/10.1016/s0957-4166(04)00209-5.

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40

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 8 (April 2004): A247—A264. http://dx.doi.org/10.1016/s0957-4166(04)00243-5.

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41

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 9 (May 2004): A265—A286. http://dx.doi.org/10.1016/s0957-4166(04)00287-3.

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42

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 10 (May 2004): A287—A313. http://dx.doi.org/10.1016/s0957-4166(04)00323-4.

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43

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 11 (June 2004): A315—A344. http://dx.doi.org/10.1016/s0957-4166(04)00383-0.

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44

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 12 (June 2004): A345—A371. http://dx.doi.org/10.1016/s0957-4166(04)00422-7.

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"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 13 (July 2004): A373—A395. http://dx.doi.org/10.1016/s0957-4166(04)00470-7.

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"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 14 (July 2004): A397—A414. http://dx.doi.org/10.1016/s0957-4166(04)00519-1.

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47

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 15 (August 2004): A415—A452. http://dx.doi.org/10.1016/s0957-4166(04)00547-6.

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48

"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 16 (August 2004): A453—A474. http://dx.doi.org/10.1016/s0957-4166(04)00608-1.

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"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 17 (September 2004): A475—A510. http://dx.doi.org/10.1016/s0957-4166(04)00651-2.

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"Stereochemistry abstracts." Tetrahedron: Asymmetry 15, no. 18 (September 2004): A511—A530. http://dx.doi.org/10.1016/s0957-4166(04)00684-6.

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