1. Philip R. Fergwon
Substituent effects on aromatic electrophilic substitution. An "experimental" class exercise
J. Chem. Educ., 1971, 48 (6), p 405
- DOI:
http://dx.doi.org/10.1021/ed048p405
Absolutely "simple" configuration in Fischer projection formula
J. Chem. Educ., 1989, 66 (6), p 480
- DOI:
http://dx.doi.org/10.1021/ed066p480
The IUPAC Rules for Naming Organic Molecules
J. Chem. Educ., 2006, 83 (11), p 1633
- DOI:
http://dx.doi.org/10.1021/ed083p1633
Hammond's postulate and the slinky
J. Chem. Educ., 1978, 55 (7), p 449
- DOI:
http://dx.doi.org/10.1021/ed055p449
Aromatic substitution reactions: when you've said ortho, meta, and para you haven't said it all
J. Chem. Educ., 1983, 60 (11), p 937
- DOI:
http://dx.doi.org/10.1021/ed060p937
Inverse Problem of Isomer Enumeration
J. Chem. Educ., 1994, 71 (6), p 512
- DOI:
http://dx.doi.org/10.1021/ed071p512
A very brief, rapid, simple, and unified method for estimating carbon-13 NMR chemical shifts: The BS method
J. Chem. Educ., 1987, 64 (11), p 915
- DOI:
http://dx.doi.org/10.1021/ed064p915
Orbital symmetry in photochemical transformations
J. Chem. Educ., 1971, 48 (2), p 84
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