Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 5 of 5 entries
Sorted by: Best Match Show Resources per page
Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones.

Organic & biomolecular chemistry

Gharui C, Prakash S, Chopra D, Pan SC.
PMID: 32236238
Org Biomol Chem. 2020 Apr 15;18(15):2828-2833. doi: 10.1039/d0ob00568a.

Herein we have developed the first enantioselective synthesis of 5-substituted-5H-benzoxathiepine-2(3H)-ones. 2-Sulfonylmethyl phenols and thioglycolates were employed as reaction partners in this method. The desired thia Michael products were obtained via bifunctional squaramide catalyzed conjugate addition reaction to in situ...

Cite
Gharui C, Prakash S, Chopra D, et al. Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones. Org Biomol Chem. 2020;18(15):2828-2833doi: 10.1039/d0ob00568a.
Gharui, C., Prakash, S., Chopra, D., & Pan, S. C. (2020). Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones. Organic & biomolecular chemistry, 18(15), 2828-2833. https://doi.org/10.1039/d0ob00568a
Gharui, Chandan, et al. "Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones." Organic & biomolecular chemistry vol. 18,15 (2020): 2828-2833. doi: https://doi.org/10.1039/d0ob00568a
Gharui C, Prakash S, Chopra D, Pan SC. Organocatalytic asymmetric addition of thioglycolates to o-quinone methides: a route to 5-substituted-5H-benzoxathiepine-2(3H)-ones. Org Biomol Chem. 2020 Apr 15;18(15):2828-2833. doi: 10.1039/d0ob00568a. PMID: 32236238.
Copy Download .nbib Format: NLM
Unilateral Koilonychia Secondary to Chemical Depilatory Product.

Skin appendage disorders

Gupta I, Tyagi M, Dayal S, Singh J.
PMID: 33614715
Skin Appendage Disord. 2021 Jan;7(1):25-28. doi: 10.1159/000510523. Epub 2020 Sep 30.

Excess hair is a problem for both men and women who want to conform to today's cosmetic social norms. Chemical depilatories are a safe, fast, and inexpensive method of hair removal. The most commonly used depilatory agents are thioglycolates...

Cite
Gupta I, Tyagi M, Dayal S, et al. Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin Appendage Disord. 2020;7(1):25-28doi: 10.1159/000510523.
Gupta, I., Tyagi, M., Dayal, S., & Singh, J. (2021). Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin appendage disorders, 7(1), 25-28. https://doi.org/10.1159/000510523
Gupta, Isha, et al. "Unilateral Koilonychia Secondary to Chemical Depilatory Product." Skin appendage disorders vol. 7,1 (2021): 25-28. doi: https://doi.org/10.1159/000510523
Gupta I, Tyagi M, Dayal S, Singh J. Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin Appendage Disord. 2021 Jan;7(1):25-28. doi: 10.1159/000510523. Epub 2020 Sep 30. PMID: 33614715; PMCID: PMC7879289.
Copy Download .nbib Format: NLM
A trial toward the synthesis of gamma-fluorinated beta-amino-alpha-thiohydroxyamino acid: a finding of desulfurizative C-C bond formation in thio-Wittig-type rearrangement of S-(N-aryl-trifluoroacetimidoyl)thioglycolates.

The Journal of organic chemistry

Uneyama K, Ohkura H, Hao J, Amii H.
PMID: 11430067
J Org Chem. 2001 Feb 09;66(3):1026-9. doi: 10.1021/jo0010330.

No abstract available.

Cite
Uneyama K, Ohkura H, Hao J, et al. A trial toward the synthesis of gamma-fluorinated beta-amino-alpha-thiohydroxyamino acid: a finding of desulfurizative C-C bond formation in thio-Wittig-type rearrangement of S-(N-aryl-trifluoroacetimidoyl)thioglycolates. J Org Chem. 2001;66(3):1026-9doi: 10.1021/jo0010330.
Uneyama, K., Ohkura, H., Hao, J., & Amii, H. (2001). A trial toward the synthesis of gamma-fluorinated beta-amino-alpha-thiohydroxyamino acid: a finding of desulfurizative C-C bond formation in thio-Wittig-type rearrangement of S-(N-aryl-trifluoroacetimidoyl)thioglycolates. The Journal of organic chemistry, 66(3), 1026-9. https://doi.org/10.1021/jo0010330
Uneyama, K, et al. "A trial toward the synthesis of gamma-fluorinated beta-amino-alpha-thiohydroxyamino acid: a finding of desulfurizative C-C bond formation in thio-Wittig-type rearrangement of S-(N-aryl-trifluoroacetimidoyl)thioglycolates." The Journal of organic chemistry vol. 66,3 (2001): 1026-9. doi: https://doi.org/10.1021/jo0010330
Uneyama K, Ohkura H, Hao J, Amii H. A trial toward the synthesis of gamma-fluorinated beta-amino-alpha-thiohydroxyamino acid: a finding of desulfurizative C-C bond formation in thio-Wittig-type rearrangement of S-(N-aryl-trifluoroacetimidoyl)thioglycolates. J Org Chem. 2001 Feb 09;66(3):1026-9. doi: 10.1021/jo0010330. PMID: 11430067.
Copy Download .nbib Format: NLM
An ethyl thioglycolate-based chemosensor: Spectrophotometric detection of Fe.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Chen ZE, Zang XF, Zhang H.
PMID: 34082353
Spectrochim Acta A Mol Biomol Spectrosc. 2021 Nov 05;260:119955. doi: 10.1016/j.saa.2021.119955. Epub 2021 May 12.

A novel symmetric bianthracene derivative (D2) containing one benzene ring and two ethyl thioglycolates connecting to the benzene ring on both sides of the bianthracene unit was designed and synthesized. D2 can detect Fe

Cite
Chen ZE, Zang XF, Zhang H. An ethyl thioglycolate-based chemosensor: Spectrophotometric detection of Fe. Spectrochim Acta A Mol Biomol Spectrosc. 2021;260:119955doi: 10.1016/j.saa.2021.119955.
Chen, Z. E., Zang, X. F., & Zhang, H. (2021). An ethyl thioglycolate-based chemosensor: Spectrophotometric detection of Fe. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 260119955. https://doi.org/10.1016/j.saa.2021.119955
Chen, Zhen-E, et al. "An ethyl thioglycolate-based chemosensor: Spectrophotometric detection of Fe." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 260 (2021): 119955. doi: https://doi.org/10.1016/j.saa.2021.119955
Chen ZE, Zang XF, Zhang H. An ethyl thioglycolate-based chemosensor: Spectrophotometric detection of Fe. Spectrochim Acta A Mol Biomol Spectrosc. 2021 Nov 05;260:119955. doi: 10.1016/j.saa.2021.119955. Epub 2021 May 12. PMID: 34082353.
Copy Download .nbib Format: NLM
Unilateral Koilonychia Secondary to Chemical Depilatory Product.

Skin appendage disorders

Gupta I, Tyagi M, Dayal S, Singh J.
PMID: 33614715
Skin Appendage Disord. 2021 Jan;7(1):25-28. doi: 10.1159/000510523. Epub 2020 Sep 30.

Excess hair is a problem for both men and women who want to conform to today's cosmetic social norms. Chemical depilatories are a safe, fast, and inexpensive method of hair removal. The most commonly used depilatory agents are thioglycolates...

Cite
Gupta I, Tyagi M, Dayal S, et al. Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin Appendage Disord. 2020;7(1):25-28doi: 10.1159/000510523.
Gupta, I., Tyagi, M., Dayal, S., & Singh, J. (2021). Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin appendage disorders, 7(1), 25-28. https://doi.org/10.1159/000510523
Gupta, Isha, et al. "Unilateral Koilonychia Secondary to Chemical Depilatory Product." Skin appendage disorders vol. 7,1 (2021): 25-28. doi: https://doi.org/10.1159/000510523
Gupta I, Tyagi M, Dayal S, Singh J. Unilateral Koilonychia Secondary to Chemical Depilatory Product. Skin Appendage Disord. 2021 Jan;7(1):25-28. doi: 10.1159/000510523. Epub 2020 Sep 30. PMID: 33614715; PMCID: PMC7879289.
Copy Download .nbib Format: NLM
Showing 1 to 5 of 5 entries