Conducting pseudopolyrotaxanes: A chemoresistive response via molecular recognition

DOI: 10.1021/ja00099a069

Source and publish data:

Journal of the American Chemical Society p. 9347 - 9348 (1994)

Update date:2022-09-26

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Authors:

Marsella, Michael J.

Carroll, Patrick J.

Swager, Timothy M.

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Article abstract of DOI:10.1021/ja00099a069

Full text of DOI:10.1021/ja00099a069

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Article Doi

Conducting pseudopolyrotaxanes: A chemoresistive response via molecular recognition

DOI: 10.1021/ja00099a069

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00099a069

Full text of DOI:10.1021/ja00099a069

Products guided by the article

R&D Labs maybe for 171085-48-6

Relevant to this article

Vinylaluminum addition to sulfinimines (N-sulfinyl imines). Asymmetric synthesis of anti-α-alkyl β-amino esters

Chiral Synthesis via Organoboranes. 42. Selective Reductions. 57. Efficient Kinetic Resolution of Representative α-Tertiary Ketones with B-Chlorodiisopinocampheylborane

Synthesis and biological evaluation of N-[4-(2-trans-[([2,6-diamino-4(3H)-oxopyrimidin-5-yl]methyl)thio]cyclo butyl)benzoyl]-L-glutamic acid a novel 5-thiepyrimidinone inhibitor of dihydrofolate reductase

Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes

Diastereoselective reduction of hemiacetals derived from 2,3-o-isopropylidene derivatives of carbohydrate lactones

p-Nitrophenyl group for anomeric protection of oligosaccharides, selective oxidative cleavage via p-acetamidophenyl glycosides