نتائج البحث - "Zavesky, Blane P"

1

Academic Journal

An attempted oxidative coupling approach to the scholarinine A framework

المؤلفون: Jones, Kerry E, Lara, Fernando Martínez, Zavesky, Blane P, Sarpong, Richmond

مصطلحات موضوعية: Organic Chemistry, Chemical Sciences, Total synthesis, Scholarinine A, Oxidative coupling, Alkaloids' akuammiline, Indole, Alkaloids’ akuammiline, Medicinal and Biomolecular Chemistry, Biochemistry and cell biology, Medicinal and biomolecular chemistry, Organic chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9m60098f
https://escholarship.org/content/qt9m60098f/qt9m60098f.pdf

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2

Academic Journal

Synthesis of Substituted 2-Aminoimidazoles via Pd-Catalyzed Alkyne Carboamination Reactions. Application to the Synthesis of Preclathridine Natural Products

المؤلفون: Zavesky, Blane P., Babij, Nicholas R., Wolfe, John P.

المساهمون: National Institutes of Health

المصدر: Organic Letters ; volume 16, issue 18, page 4952-4955 ; ISSN 1523-7060 1523-7052

الاتاحة: http://dx.doi.org/10.1021/ol502471x
https://pubs.acs.org/doi/pdf/10.1021/ol502471x

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3

Academic Journal

Thioetherification of Aryl Halides with Thioacetates.

المؤلفون: Hopkins, Brett Andrew, Zavesky, Blane, White, Derick

المصدر: Journal of Organic Chemistry; 6/3/2022, Vol. 87 Issue 11, p7547-7550, 4p

4

Academic Journal

Progress toward a Convergent, Asymmetric Synthesis of Jervine

المؤلفون: Zavesky, Blane P., De Jesús Cruz, Pedro, Johnson, Jeffrey S.

المساهمون: Division of Chemistry, National Institute of General Medical Sciences

المصدر: Organic Letters ; volume 22, issue 9, page 3537-3541 ; ISSN 1523-7060 1523-7052

الاتاحة: http://dx.doi.org/10.1021/acs.orglett.0c00972
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c00972

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5

Academic Journal

Direct Zinc(II)‐Catalyzed Enantioconvergent Additions of Terminal Alkynes to α‐Keto Esters

المؤلفون: Zavesky, Blane P., Johnson, Jeffrey S.

المساهمون: National Institute of General Medical Sciences

المصدر: Angewandte Chemie International Edition ; volume 56, issue 30, page 8805-8808 ; ISSN 1433-7851 1521-3773

الاتاحة: http://dx.doi.org/10.1002/anie.201704226
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201704226
https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201704226

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6

Academic Journal

Palladium-Catalyzed β-Arylation of α-Keto Esters

المؤلفون: Zavesky, Blane P., Bartlett, Samuel L., Johnson, Jeffrey S.

المساهمون: National Institute of General Medical Sciences

المصدر: Organic Letters ; volume 19, issue 8, page 2126-2129 ; ISSN 1523-7060 1523-7052

الاتاحة: http://dx.doi.org/10.1021/acs.orglett.7b00761
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b00761

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7

Academic Journal

Asymmetric Organocatalytic Reductive Coupling Reactions between Benzylidene Pyruvates and Aldehydes

المؤلفون: Horwitz, Matthew A., Zavesky, Blane P., Martinez-Alvarado, Jesus I., Johnson, Jeffrey S.

المصدر: Organic Letters, 18(1)

مصطلحات موضوعية: Aldehydes, dimethyl hydrogen phosphite, Benzylidene Compounds, Phosphites, Molecular Structure, Stereoisomerism, Catalysis, Organophosphonates, Pyruvates

Relation: https://doi.org/10.17615/v6sg-0p08; https://cdr.lib.unc.edu/downloads/9019s715p?file=thumbnail; https://cdr.lib.unc.edu/downloads/9019s715p

الاتاحة: https://doi.org/10.17615/v6sg-0p08
https://cdr.lib.unc.edu/downloads/9019s715p?file=thumbnail
https://cdr.lib.unc.edu/downloads/9019s715p

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8

Academic Journal

ChemInform Abstract: Asymmetric Organocatalytic Reductive Coupling Reactions Between Benzylidene Pyruvates and Aldehydes.

المؤلفون: Horwitz, Matthew A., Zavesky, Blane P., Martinez‐Alvarado, Jesus I., Johnson, Jeffrey S.

المصدر: ChemInform ; volume 47, issue 20 ; ISSN 0931-7597 1522-2667

الاتاحة: http://dx.doi.org/10.1002/chin.201620190
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201620190
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.201620190

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9

Academic Journal

ChemInform Abstract: Synthesis of Substituted 2‐Aminoimidazoles via Pd‐Catalyzed Alkyne Carboamination Reactions. Application to the Synthesis of Preclathridine Natural Products.

المؤلفون: Zavesky, Blane P., Babij, Nicholas R., Wolfe, John P.

المصدر: ChemInform ; volume 46, issue 12 ; ISSN 0931-7597 1522-2667

الاتاحة: http://dx.doi.org/10.1002/chin.201512184
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201512184
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.201512184

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10

Academic Journal

Asymmetric Organocatalytic Reductive Coupling Reactions between Benzylidene Pyruvates and Aldehydes

المؤلفون: Horwitz, Matthew A., Zavesky, Blane P., Martinez-Alvarado, Jesus I., Johnson, Jeffrey S.

المساهمون: National Institute of General Medical Sciences

المصدر: Organic Letters ; volume 18, issue 1, page 36-39 ; ISSN 1523-7060 1523-7052

الاتاحة: http://dx.doi.org/10.1021/acs.orglett.5b03127
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b03127

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11

Academic Journal

ChemInform Abstract: Synthesis of Cyclic Guanidines via Pd‐Catalyzed Alkene Carboamination.

المؤلفون: Zavesky, Blane P., Babij, Nicholas R., Fritz, Jonathan A., Wolfe, John P.

المصدر: ChemInform ; volume 45, issue 11 ; ISSN 0931-7597 1522-2667

الاتاحة: http://dx.doi.org/10.1002/chin.201411087
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201411087
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.201411087

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12

Academic Journal

Synthesis of Cyclic Guanidines via Pd-Catalyzed Alkene Carboamination

المؤلفون: Zavesky, Blane P., Babij, Nicholas R., Fritz, Jonathan A., Wolfe, John P.

المساهمون: National Institutes of Health

المصدر: Organic Letters ; volume 15, issue 21, page 5420-5423 ; ISSN 1523-7060 1523-7052

الاتاحة: http://dx.doi.org/10.1021/ol402377y
https://pubs.acs.org/doi/pdf/10.1021/ol402377y

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13

Academic Journal

Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement of α-Keto Ester Derived Nitrones.

المؤلفون: Bartlett, Samuel L., Keiter, Kimberly M., Zavesky, Blane P., Johnson, Jeffrey S.

المصدر: Synthesis; 2019, Vol. 51 Issue 1, p203-212, 10p

مصطلحات موضوعية: BENZOYL compounds, NITRONES, AMINO alcohols, ALCOHOLS (Chemical class), ACYL compounds

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