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Synthesis of limonoid natural products
B Heasley - European Journal of Organic Chemistry, 2011 - Wiley Online Library
Limonoid natural products are a large family of oxygenated terpenoid compounds that are
best known as secondary metabolites found in citrus fruit. The diverse array of significant …
best known as secondary metabolites found in citrus fruit. The diverse array of significant …
Collective Synthesis of Lycopodium Alkaloids and Tautomer Locking Strategy for the Total Synthesis of (−)-Lycojapodine A
The collective total synthesis of Lycopodium alkaloids (+)-fawcettimine (1),(+)-fawcettidine
(2),(+)-alopecuridine (4),(−)-lycojapodine A (6), and (−)-8-deoxyserratinine (7) has been …
(2),(+)-alopecuridine (4),(−)-lycojapodine A (6), and (−)-8-deoxyserratinine (7) has been …
Synthesis of the [7-5-5] tricyclic core of Daphniphyllum alkaloids
Y Kitabayashi, T Fukuyama… - Organic & Biomolecular …, 2018 - pubs.rsc.org
The [7-5-5] tricyclic core of the Daphniphyllum alkaloids was constructed, featuring a Claisen-
Ireland rearrangement to install the two contiguous stereogenic centers, E1cB elimination to …
Ireland rearrangement to install the two contiguous stereogenic centers, E1cB elimination to …
Gold (I)‐Catalyzed Tandem Cycloisomerization of 1, 5‐Enyne Ethers by Hydride Transfer
XL Lu, MY Lyu, XS Peng, HNC Wong - Angewandte Chemie, 2018 - Wiley Online Library
A novel gold‐catalyzed tandem protocol, initiated by hydride transfer in the presence of
catalytic (C6F5) 3PAuCl/AgSbF6, for the formation of fused polycyclic ring systems has been …
catalytic (C6F5) 3PAuCl/AgSbF6, for the formation of fused polycyclic ring systems has been …
Total synthesis of (±)-pallambins C and D
The first total synthesis of (±)-pallambins C and D has been accomplished in a linear 38 step
reaction from (±)-Wieland–Miescher ketone. The key conversions are featured as follows: a …
reaction from (±)-Wieland–Miescher ketone. The key conversions are featured as follows: a …
Highly regio-and stereoselective synthesis of tricyclic frameworks using Baylis–Hillman derivatives
Highly regio- and stereoselective synthesis of tricyclic frameworks using Baylis–Hillman
derivatives - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & …
derivatives - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & …
A biosynthetically inspired synthesis of (−)-berkelic acid and analogs
CF Bender, CL Paradise, VM Lynch, FK Yoshimoto… - Tetrahedron, 2018 - Elsevier
We describe a complete account of our total synthesis and biological evaluation of (−)-
berkelic acid and analogs. We delineate a synthetic strategy inspired by a potentially …
berkelic acid and analogs. We delineate a synthetic strategy inspired by a potentially …
Formal Synthesis of Aspidospermidine via the Intramolecular Cascade Transannular Cyclization
JZ Huang, XK Jie, K Wei, H Zhang, MC Wang… - Synlett, 2013 - thieme-connect.com
A formal synthesis of aspidospermidine is reported through a novel preparation of Stork's
penultimate tricyclic ketone intermediate. The key steps of the synthesis consist of an …
penultimate tricyclic ketone intermediate. The key steps of the synthesis consist of an …
Total synthesis of (+)-aplykurodinone-1
B Xu, W Xun, T Wang, FG Qiu - Organic letters, 2017 - ACS Publications
Starting from (R)-citronellic acid and (R)-seudenol, the total synthesis of (+)-aplykurodinone-
1, a highly degraded marine steroid, has been achieved in 11 steps and in 19% overall yield …
1, a highly degraded marine steroid, has been achieved in 11 steps and in 19% overall yield …
Cyclization Approaching to (−)-Lycojapodine A: Synthesis of Two Unnatural Alkaloids
YR Yang, L Shen, K Wei, QS Zhao - The Journal of Organic …, 2010 - ACS Publications
Cyclization Approaching to (−)-Lycojapodine A: Synthesis of Two Unnatural Alkaloids | The
Journal of Organic Chemistry Recently Viewedclose modal ACS ACS Publications C&EN CAS …
Journal of Organic Chemistry Recently Viewedclose modal ACS ACS Publications C&EN CAS …