Catalytic Enantioselective Aza-pinacol Rearrangement.

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Copper-Catalyzed Enantioselective Domino Arylation/Semipinacol Rearrangement of Allylic Alcohols with Diaryliodonium Salts.

P2860

Q47863934-8EF2A6AE-AA8C-4B14-BCB9-019B16EC6D2F

P2860

Catalytic Enantioselective Aza-pinacol Rearrangement.

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http://www.wikidata.org/entity/Q48271486

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Catalytic Enantioselective Aza-pinacol Rearrangement.

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Catalytic Enantioselective Aza-pinacol Rearrangement.

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type

Item

label

Catalytic Enantioselective Aza-pinacol Rearrangement.

@en

Catalytic Enantioselective Aza-pinacol Rearrangement.

@nl

prefLabel

Catalytic Enantioselective Aza-pinacol Rearrangement.

@en

Catalytic Enantioselective Aza-pinacol Rearrangement.

@nl

P1476

Catalytic Enantioselective Aza-pinacol Rearrangement.

@en

P2093

Jing-Ren Zhang

http://www.w3.org/2001/XMLSchema#string

Jingwen Li

http://www.w3.org/2001/XMLSchema#string

Long Jiang

http://www.w3.org/2001/XMLSchema#string

Yuanyuan Yu

http://www.w3.org/2001/XMLSchema#string

P2860

Molecular rearrangements in the construction of complex molecules

Semipinacol Rearrangement in Natural Product Synthesis

Structure-activity relationship studies of the tricyclic indoline resistance-modifying agent.

Total synthesis of the strychnos alkaloid (+)-minfiensine: tandem enantioselective intramolecular Heck-iminium ion cyclization.

Bio-inspired synthesis yields a tricyclic indoline that selectively resensitizes methicillin-resistant Staphylococcus aureus (MRSA) to β-lactam antibiotics

Current progress in the chemistry and pharmacology of akuammiline alkaloids.

Discovery and initial structure-activity relationships of N-benzyl tricyclic indolines as antibacterials for methicillin-resistant Staphylococcus aureus.

Recent advances in the semi-pinacol rearrangement of alpha-hydroxy epoxides and related compounds.

Chiral Brønsted acids in enantioselective carbonyl activations--activation modes and applications.

Access to the Pyrroloindoline Core via [3 + 2] Annulation as well as the Application in the Synthetic Approach to (±)-Minfiensine.

P304

9217-9221

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P31

scholarly article

P356

10.1002/ANIE.201705539

http://www.w3.org/2001/XMLSchema#string

P407

English

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http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Liansuo Zu

P577

2017-06-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28618154

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P921

enantioselectivity

Catalytic Enantioselective Aza-pinacol Rearrangement.

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P2860

P2860

Catalytic Enantioselective Aza-pinacol Rearrangement.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921