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Start Over Author "He, Chi" Journal journal of the american chemical society
10 results on '"He, Chi"'

1. Divergent Synthetic Approach to Grayanane Diterpenoids

Author

Zhu, An, primary, Lyu, Yumeng, additional, Xia, Qidong, additional, Wu, Yufei, additional, Tang, Dongmin, additional, He, Chi, additional, Zheng, Guijuan, additional, Feng, Yuanyuan, additional, Wang, Yong, additional, Yao, Guangmin, additional, and Ding, Hanfeng, additional

Published
2023
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4. N-Ammonium Ylide Mediators for Electrochemical C–H Oxidation

Author

Saito, Masato, primary, Kawamata, Yu, additional, Meanwell, Michael, additional, Navratil, Rafael, additional, Chiodi, Debora, additional, Carlson, Ethan, additional, Hu, Pengfei, additional, Chen, Longrui, additional, Udyavara, Sagar, additional, Kingston, Cian, additional, Tanwar, Mayank, additional, Tyagi, Sameer, additional, McKillican, Bruce P., additional, Gichinga, Moses G., additional, Schmidt, Michael A., additional, Eastgate, Martin D., additional, Lamberto, Massimiliano, additional, He, Chi, additional, Tang, Tianhua, additional, Malapit, Christian A., additional, Sigman, Matthew S., additional, Minteer, Shelley D., additional, Neurock, Matthew, additional, and Baran, Phil S., additional

Published
2021
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5. Total Synthesis of Tagetitoxin

Author

He, Chi, primary, Chu, Hang, additional, Stratton, Thomas P., additional, Kossler, David, additional, Eberle, Kelly J., additional, Flood, Dillon T., additional, and Baran, Phil S., additional

Published
2020
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8. Total Synthesis of (−)-Rhodomollanol A

Author

Gao, Jianhong, Rao, Peirong, Xu, Kaixiang, Wang, Shuaifeng, Wu, Yufei, He, Chi, and Ding, Hanfeng

Abstract

An asymmetric approach for the first total synthesis of (−)-rhodomollanol A, a highly oxidized diterpenoid, is described. The efficient synthetic strategy features three key transformations: (1) an oxidative dearomatization-induced (5 + 2) cycloaddition/pinacol-type 1,2-acyl migration cascade to build up the bicyclo[3.2.1]octane skeleton; (2) a retro-Dieckmann fragmentation/vinylogous Dieckmann cyclization cascade to assemble the bicyclo[3.3.0]octane subunit; and (3) a photo-Nazarov cyclization/intramolecular cycloetherification cascade to forge the 7-oxabicyclo[4.2.1]nonane core structure of the natural product.

Published
2020
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10. Total Synthesis of (-)-Rhodomollanol A.

Author

Gao J, Rao P, Xu K, Wang S, Wu Y, He C, and Ding H

Subjects
Cycloaddition Reaction, Oxidation-Reduction, Stereoisomerism, Diterpenes chemical synthesis
Abstract

An asymmetric approach for the first total synthesis of (-)-rhodomollanol A, a highly oxidized diterpenoid, is described. The efficient synthetic strategy features three key transformations: (1) an oxidative dearomatization-induced (5 + 2) cycloaddition/pinacol-type 1,2-acyl migration cascade to build up the bicyclo[3.2.1]octane skeleton; (2) a retro -Dieckmann fragmentation/vinylogous Dieckmann cyclization cascade to assemble the bicyclo[3.3.0]octane subunit; and (3) a photo-Nazarov cyclization/intramolecular cycloetherification cascade to forge the 7-oxabicyclo[4.2.1]nonane core structure of the natural product.

Published
2020
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