Sufficient training data normally is required to train deeply learned models. However, due to the expensive manual process for labelling large number of images (i.e., annotation), the amount of available training data (i.e., real data) is always limited. To produce more data for training a deep network, Generative Adversarial Network (GAN) can be used to generate artificial sample data (i.e., generated data). However, the generated data usually does not have annotation labels. To solve this problem, in this paper, we propose a virtual label called Multi-pseudo Regularized Label (MpRL) and assign it to the generated data. With MpRL, the generated data will be used as the supplementary of real training data to train a deep neural network in a semi-supervised learning fashion. To build the corresponding relationship between the real data and generated data, MpRL assigns each generated data a proper virtual label which reflects the likelihood of the affiliation of the generated data to pre-defined training classes in the real data domain. Unlike the traditional label which usually is a single integral number, the virtual label proposed in this work is a set of weight-based values each individual of which is a number in (0,1] called multi-pseudo label and reflects the degree of relation between each generated data to every pre-defined class of real data.A comprehensive evaluation is carried out by adopting two state-of-the-art convolutional neural networks (CNNs) in our experiments to verify the effectiveness of MpRL. Experiments demonstrate that by assigning MpRL to generated data, we can further improve the person re-ID performance on five re-ID datasets, i.e., Market-1501, DukeMTMC-reID, CUHK03, VIPeR, and CUHK01. The proposed method obtains +6.29%, +6.30%, +5.58%, +5.84%, and +3.48% improvements in rank-1 accuracy over a strong CNN baseline on the five datasets respectively, and outperforms state-of-the-art methods.

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Convolutional sparse coding (CSC) can model local connections between image content and reduce the code redundancy when compared with patch-based sparse coding. However, CSC needs a complicated optimization procedure to infer the codes (i.e., feature maps). In this brief, we proposed a convolutional sparse auto-encoder (CSAE), which leverages the structure of the convolutional AE and incorporates the max-pooling to heuristically sparsify the feature maps for feature learning. Together with competition over feature channels, this simple sparsifying strategy makes the stochastic gradient descent algorithm work efficiently for the CSAE training; thus, no complicated optimization procedure is involved. We employed the features learned in the CSAE to initialize convolutional neural networks for classification and achieved competitive results on benchmark data sets. In addition, by building connections between the CSAE and CSC, we proposed a strategy to construct local descriptors from the CSAE for classification. Experiments on Caltech-101 and Caltech-256 clearly demonstrated the effectiveness of the proposed method and verified the CSAE as a CSC model has the ability to explore connections between neighboring image content for classification tasks.

Main observation and conclusion Herein, we report an efficient, tunable system for electrochemical reduction of ketones and phthalimides at room temperature without the need for stoichiometric external reductants. By utilizing NaN3 as the electrolyte and graphite felt as both the cathode and the anode, we were able to selectively reduce the carbonyl groups of the substrates to alcohols, pinacols, or methylene groups by judiciously choosing the solvent and an acidic additive. The reaction conditions were compatible with a diverse array of functional groups, and phthalimides could undergo one‐pot reductive cyclization to afford products with indolizidine scaffolds. Mechanistic studies showed that the reactions involved electron, proton, and hydrogen atom transfers. Importantly, an N3/HN3 cycle operated as a hydrogen atom shuttle, which was critical for reduction of the carbonyl groups to methylene groups.