نتائج البحث - "Nambu, Hisanori"

المساهمون: Ministry of Education, Culture, Sports, Science and Technology, Kyoto Pharmaceutical University, Japan Society for the Promotion of Science

المصدر: Journal of Medicinal Chemistry ; volume 66, issue 9, page 6403-6413 ; ISSN 0022-2623 1520-4804

الاتاحة: http://dx.doi.org/10.1021/acs.jmedchem.3c00474
https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.3c00474

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9

Academic Journal

Corrigendum to “Recent topics in application of selective Rh(II)-catalyzed C H functionalization toward natural product synthesis” [Tetrahedron Lett 59 (2018) 188–202]

المؤلفون: Yakura, Takayuki, Nambu, Hisanori

المصدر: Tetrahedron Letters ; volume 59, issue 50, page 4448 ; ISSN 0040-4039

الاتاحة: https://doi.org/10.1016/j.tetlet.2018.10.072
https://api.elsevier.com/content/article/PII:S0040403918313133?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0040403918313133?httpAccept=text/plain

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10

Academic Journal

Structural and thermodynamic analyses reveal critical features of glycopeptide recognition by the human PILRα immune cell receptor

المؤلفون: Furukawa Atsushi, Kakita Kosuke, Yamada Tomoki, Ishizuka Mikihiro, Sakamoto Jiro, Hatori Nanao, Maeda Naoyoshi, Ohsaka Fumina, Saitoh Takashi, Nomura Takahiro, Kuroki Kimiko, Nambu Hisanori, Arase Hisashi, Matsunaga Shigeki, Anada Masahiro, Ose Toyoyuki, Hashimoto Shunichi, Maenaka Katsumi, 古川敦

Relation: https://www.sciencedirect.com/science/article/pii/S0021925820327617?via%3Dihub; https://www.journals.elsevier.com/journal-of-biological-chemistry; http://www.asbmb.org/; https://kanazawa-u.repo.nii.ac.jp/?action=repository_uri&item_id=60836; http://hdl.handle.net/2297/00067081; Journal of Biological Chemistry, 292(51), 21128-21136(2017-12-22); AA00251083; https://kanazawa-u.repo.nii.ac.jp/?action=repository_action_common_download&item_id=60836&item_no=1&attribute_id=26&file_no=1

الاتاحة: http://hdl.handle.net/2297/00067081
https://kanazawa-u.repo.nii.ac.jp/?action=repository_uri&item_id=60836
https://kanazawa-u.repo.nii.ac.jp/?action=repository_action_common_download&item_id=60836&item_no=1&attribute_id=26&file_no=1

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11

Academic Journal

Cover Feature: An Efficient Route to Highly Substituted Indoles via Tetrahydroindol‐4(5 H)‐one Intermediates Produced by Ring‐Opening Cyclization of Spirocyclopropanes with Amines (Chem. Eur. J. 66/2017)

المؤلفون: Nambu, Hisanori, Hirota, Wataru, Fukumoto, Masahiro, Tamura, Takafumi, Yakura, Takayuki

المصدر: Chemistry – A European Journal ; volume 23, issue 66, page 16693-16693 ; ISSN 0947-6539 1521-3765

الاتاحة: http://dx.doi.org/10.1002/chem.201704085
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchem.201704085
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201704085

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12

Academic Journal

Structural and thermodynamic analyses reveal critical features of glycopeptide recognition by the human PILRα immune cell receptor

المؤلفون: Furukawa, Atsushi, Kakita, Kosuke, Yamada, Tomoki, Ishizuka, Mikihiro, Sakamoto, Jiro, Hatori, Nanao, Maeda, Naoyoshi, Ohsaka, Fumina, Saitoh, Takashi, Nomura, Takao, Kuroki, Kimiko, Nambu, Hisanori, Arase, Hisashi, Matsunaga, Shigeki, Anada, Masahiro, Ose, Toyoyuki, Hashimoto, Shunichi, Maenaka, Katsumi

المصدر: Journal of Biological Chemistry ; volume 292, issue 51, page 21128-21136 ; ISSN 0021-9258

الاتاحة: http://dx.doi.org/10.1074/jbc.m117.799239
https://api.elsevier.com/content/article/PII:S0021925820327617?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0021925820327617?httpAccept=text/plain
https://syndication.highwire.org/content/doi/10.1074/jbc.M117.799239

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13

Academic Journal

Rhodium(II)‐Catalyzed Site‐Selective Intramolecular Insertion of Aryldiazoacetates into Unactivated Primary C−H Bond: A Direct Route to 2‐Unsubstituted Indanes

المؤلفون: Nambu, Hisanori, Amano, Ryoya, Tamura, Takafumi, Yakura, Takayuki

المساهمون: Ministry of Education, Culture, Sports, Science and Technology

المصدر: Advanced Synthesis & Catalysis ; volume 364, issue 14, page 2422-2428 ; ISSN 1615-4150 1615-4169

الاتاحة: http://dx.doi.org/10.1002/adsc.202200115
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200115
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/adsc.202200115

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14

A Concise and Protecting-Group-Free Formal Synthesis of Aspidospermidine: Ring-Opening Cyclization of Spirocyclopropane with Amine Followed by Regioselective Alkylations

المؤلفون: Nambu, Hisanori, Tamura, Takafumi, Yakura, Takayuki

المصدر: Journal of Organic Chemistry. 84(24):15990-15996

URL الوصول: https://explore.openaire.eu/search/publication?articleId=jairo_______::d70050137504563afa21ece6619d860d
http://hdl.handle.net/10110/00020542

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15

Academic Journal

Ring-Opening Cyclization of Spirocyclopropanes Using Sulfoxonium Ylides

المؤلفون: onuki yuta, Nambu Hisanori, Yakura Takayuki

Relation: https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18102; http://hdl.handle.net/10110/00020538; Chemical and Pharmaceutical Bulletin, 68, 479-486(2020-05-01); https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18102&item_no=1&attribute_id=18&file_no=1

الاتاحة: http://hdl.handle.net/10110/00020538
https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18102
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18102&item_no=1&attribute_id=18&file_no=1

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16

Electronic Resource

A Concise and Protecting-Group-Free Formal Synthesis of Aspidospermidine: Ring-Opening Cyclization of Spirocyclopropane with Amine Followed by Regioselective Alkylations

المؤلفون: Nambu, Hisanori, Tamura, Takafumi, Yakura, Takayuki

مصطلحات الفهرس: Journal Article, AM

URL: http://hdl.handle.net/10110/00020542
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18106&item_no=1&attribute_id=18&file_no=1
https://doi.org/10.1021/acs.joc.9b02469
https://doi.org/10.1021/acs.joc.9b02469

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17

Electronic Resource

Ring-Opening Cyclization of Spirocyclopropanes Using Sulfoxonium Ylides

المؤلفون: onuki, yuta, Nambu, Hisanori, Yakura, Takayuki

مصطلحات الفهرس: Journal Article, VoR

URL: http://hdl.handle.net/10110/00020538
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18102&item_no=1&attribute_id=18&file_no=1

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18

Electronic Resource

Ring‐opening cyclization of spirocyclopropanes with stabilized sulfonium ylides for the construction of a chromane skeleton

المؤلفون: Nambu, Hisanori, onuki, yuta, Ono, Naoki, Tsuge, Kiyoshi, Yakura, Takayuki

مصطلحات الفهرس: Journal Article, AM

URL: http://hdl.handle.net/10110/00020541
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18105&item_no=1&attribute_id=18&file_no=1
https://doi.org/10.1039/C9CC03023A
https://doi.org/10.1039/C9CC03023A

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19

Academic Journal

A Concise and Protecting-Group-Free Formal Synthesis of Aspidospermidine: Ring-Opening Cyclization of Spirocyclopropane with Amine Followed by Regioselective Alkylations

المؤلفون: Nambu Hisanori, Tamura Takafumi, Yakura Takayuki

Relation: https://doi.org/10.1021/acs.joc.9b02469; https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18106; http://hdl.handle.net/10110/00020542; Journal of Organic Chemistry , 84(24), 15990-15996(2019-11-20); https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18106&item_no=1&attribute_id=18&file_no=1

الاتاحة: http://hdl.handle.net/10110/00020542
https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18106
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18106&item_no=1&attribute_id=18&file_no=1

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20

Academic Journal

Ring‐opening cyclization of spirocyclopropanes with stabilized sulfonium ylides for the construction of a chromane skeleton

المؤلفون: Nambu Hisanori, onuki yuta, Ono Naoki, Tsuge Kiyoshi, Yakura Takayuki

Relation: https://doi.org/10.1039/C9CC03023A; https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18105; http://hdl.handle.net/10110/00020541; Chemical Communications , 46, 6539-6542(2019-05-14); https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18105&item_no=1&attribute_id=18&file_no=1

الاتاحة: http://hdl.handle.net/10110/00020541
https://toyama.repo.nii.ac.jp/?action=repository_uri&item_id=18105
https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=18105&item_no=1&attribute_id=18&file_no=1

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